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nsv1191416

  • Variant Calls:15
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,747,097

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 11080 SVs from 132 studies. See in: genome view    
Remapped(Score: Pass):18,339,130-21,086,226Question Mark
Overlapping variant regions from other studies: 10115 SVs from 129 studies. See in: genome view    
Remapped(Score: Good):18,919,941-21,440,515Question Mark
Overlapping variant regions from other studies: 3604 SVs from 35 studies. See in: genome view    
Submitted genomic17,299,941-19,770,515Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1191416RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2218,339,13021,086,226
nsv1191416RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2218,919,94121,440,515
nsv1191416Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000022.9Chr2217,299,94119,770,515

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv7462632copy number loss19325Oligo aCGHProbe signal intensitynssv7460109
nssv7463627copy number loss24273Oligo aCGHProbe signal intensitynssv7466491
nssv7464465copy number loss14988Oligo aCGHProbe signal intensitynssv7462756
nssv7464800copy number loss23187Oligo aCGHProbe signal intensitynssv7466025
nssv7464843copy number loss24308Oligo aCGHProbe signal intensitynssv7471421
nssv7465217copy number loss19267Oligo aCGHProbe signal intensitynssv7470738
nssv7466552copy number loss15144Oligo aCGHProbe signal intensitynssv7469617
nssv7467060copy number loss24473Oligo aCGHProbe signal intensitynssv7471507, nssv7465860
nssv7467233copy number loss20745Oligo aCGHProbe signal intensitynssv7461994, nssv7467086
nssv7468761copy number gain30139Oligo aCGHProbe signal intensity5
nssv7472388copy number gain16699Oligo aCGHProbe signal intensitynssv7459304, nssv7471009
nssv7472782copy number loss16715Oligo aCGHProbe signal intensitynssv7464012
nssv7473561copy number loss31862Oligo aCGHProbe signal intensitynssv7467269, nssv7470612, nssv7468798
nssv7473720copy number loss18026Oligo aCGHProbe signal intensitynssv7465516
nssv7474950copy number gain30496Oligo aCGHProbe signal intensitynssv7466623

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv7462632RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7463627RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7464465RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7464800RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7464843RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7465217RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7466552RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7467060RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7467233RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7468761RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)dup
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7472388RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)dup
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7472782RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7473561RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7473720RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)del
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7474950RemappedPassNC_000022.11:g.(?_
18339130)_(2108622
6_?)dup
GRCh38.p12First PassNC_000022.11Chr2218,339,13021,086,226
nssv7462632RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7463627RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7464465RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7464800RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7464843RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7465217RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7466552RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7467060RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7467233RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7468761RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)dup
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7472388RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)dup
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7472782RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7473561RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7473720RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)del
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7474950RemappedGoodNC_000022.10:g.(?_
18919941)_(2144051
5_?)dup
GRCh37.p13First PassNC_000022.10Chr2218,919,94121,440,515
nssv7462632Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7463627Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7464465Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7464800Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7464843Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7465217Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7466552Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7467060Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7467233Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7468761Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)dup
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7472388Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)dup
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7472782Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7473561Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7473720Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)del
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515
nssv7474950Submitted genomicNC_000022.9:g.(?_1
7299941)_(19770515
_?)dup
NCBI36 (hg18)NC_000022.9Chr2217,299,94119,770,515

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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