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nsv888239

  • Variant Calls:20
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73,262

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 302 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):63,401,698-63,474,959Question Mark
Overlapping variant regions from other studies: 310 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):62,862,076-62,935,337Question Mark
Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
Submitted genomic62,499,511-62,572,772Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv888239RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nsv888239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nsv888239Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr762,499,51162,510,88862,563,43162,572,772

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1520612copy number lossSP51179SNP arraySNP genotyping analysis18
nssv1520875copy number lossSP51290SNP arraySNP genotyping analysis14
nssv1522786copy number lossSP53426SNP arraySNP genotyping analysis12
nssv1525253copy number lossSP56381SNP arraySNP genotyping analysis14
nssv1525394copy number lossSP56542SNP arraySNP genotyping analysis11
nssv1531671copy number lossMS10591SNP arraySNP genotyping analysis18
nssv1532852copy number lossMS10875SNP arraySNP genotyping analysis7
nssv1534957copy number lossMS11858SNP arraySNP genotyping analysis15
nssv1538915copy number lossMS13813SNP arraySNP genotyping analysis9
nssv1545347copy number lossMS16728SNP arraySNP genotyping analysis9
nssv1545588copy number lossMS16846SNP arraySNP genotyping analysis10
nssv1549462copy number lossMS18247SNP arraySNP genotyping analysis13
nssv1550505copy number lossMS18432SNP arraySNP genotyping analysis8
nssv1550629copy number lossMS18503SNP arraySNP genotyping analysis14
nssv1554268copy number lossMS20702SNP arraySNP genotyping analysis12
nssv1557853copy number lossMS22952SNP arraySNP genotyping analysis10
nssv1558907copy number lossMS23626SNP arraySNP genotyping analysis14
nssv1560245copy number lossMS24390SNP arraySNP genotyping analysis12
nssv1560505copy number lossMS24508SNP arraySNP genotyping analysis13
nssv1562449copy number lossMS25589SNP arraySNP genotyping analysis13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1520612RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1520875RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1522786RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1525253RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1525394RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1531671RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1532852RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1534957RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1538915RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1545347RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1545588RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1549462RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1550505RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1550629RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1554268RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1557853RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1558907RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1560245RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1560505RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1562449RemappedPerfectNC_000007.14:g.(63
401698_63413075)_(
63465618_63474959)
del
GRCh38.p12First PassNC_000007.14Chr763,401,69863,413,07563,465,61863,474,959
nssv1520612RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1520875RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1522786RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1525253RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1525394RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1531671RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1532852RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1534957RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1538915RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1545347RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1545588RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1549462RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1550505RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1550629RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1554268RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1557853RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1558907RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1560245RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1560505RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1562449RemappedPerfectNC_000007.13:g.(62
862076_62873453)_(
62925996_62935337)
del
GRCh37.p13First PassNC_000007.13Chr762,862,07662,873,45362,925,99662,935,337
nssv1520612Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1520875Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1522786Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1525253Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1525394Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1531671Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1532852Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1534957Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1538915Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1545347Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1545588Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1549462Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1550505Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1550629Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1554268Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1557853Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1558907Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1560245Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1560505Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772
nssv1562449Submitted genomicNC_000007.12:g.(62
499511_62510888)_(
62563431_62572772)
del
NCBI36 (hg18)NC_000007.12Chr762,499,51162,510,88862,563,43162,572,772

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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