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nsv879418

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:104,491

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1346 SVs from 100 studies. See in: genome view    
Remapped(Score: Perfect):69,264,211-69,368,701Question Mark
Overlapping variant regions from other studies: 1346 SVs from 100 studies. See in: genome view    
Remapped(Score: Perfect):70,129,929-70,234,419Question Mark
Overlapping variant regions from other studies: 743 SVs from 35 studies. See in: genome view    
Submitted genomic70,164,518-70,269,008Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv879418RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nsv879418RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nsv879418Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr470,164,51870,166,45370,257,47170,269,008

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1499263copy number lossSP50521SNP arraySNP genotyping analysis28
nssv1499334copy number lossSP50103SNP arraySNP genotyping analysis11
nssv1502304copy number gainSP51062SNP arraySNP genotyping analysis10
nssv1503253copy number lossSP52019SNP arraySNP genotyping analysis22
nssv1503627copy number lossSP52082SNP arraySNP genotyping analysis15
nssv1503647copy number lossSP52093SNP arraySNP genotyping analysis35
nssv1503751copy number lossSP52109SNP arraySNP genotyping analysis18
nssv1505011copy number lossSP53036SNP arraySNP genotyping analysis14
nssv1505037copy number lossSP53041SNP arraySNP genotyping analysis60
nssv1506649copy number lossSP54384SNP arraySNP genotyping analysis18
nssv1506667copy number lossSP54389SNP arraySNP genotyping analysis19
nssv1506856copy number lossSP54409SNP arraySNP genotyping analysis20
nssv1513666copy number lossSP55822SNP arraySNP genotyping analysis16
nssv1515209copy number lossSP56138SNP arraySNP genotyping analysis20
nssv1517559copy number lossSP57322SNP arraySNP genotyping analysis21
nssv1518011copy number lossSP57443SNP arraySNP genotyping analysis18
nssv1518359copy number lossSP57507SNP arraySNP genotyping analysis16

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1499263RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1499334RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1502304RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
dup
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1503253RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1503627RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1503647RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1503751RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1505011RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1505037RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1506649RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1506667RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1506856RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1513666RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1515209RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1517559RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1518011RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1518359RemappedPerfectNC_000004.12:g.(69
264211_69266146)_(
69357164_69368701)
del
GRCh38.p12First PassNC_000004.12Chr469,264,21169,266,14669,357,16469,368,701
nssv1499263RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1499334RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1502304RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
dup
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1503253RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1503627RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1503647RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1503751RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1505011RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1505037RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1506649RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1506667RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1506856RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1513666RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1515209RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1517559RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1518011RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1518359RemappedPerfectNC_000004.11:g.(70
129929_70131864)_(
70222882_70234419)
del
GRCh37.p13First PassNC_000004.11Chr470,129,92970,131,86470,222,88270,234,419
nssv1499263Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1499334Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1502304Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
dup
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1503253Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1503627Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1503647Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1503751Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1505011Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1505037Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1506649Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1506667Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1506856Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1513666Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1515209Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1517559Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1518011Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008
nssv1518359Submitted genomicNC_000004.10:g.(70
164518_70166453)_(
70257471_70269008)
del
NCBI36 (hg18)NC_000004.10Chr470,164,51870,166,45370,257,47170,269,008

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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