A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516773



Internal ID15097380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161721643..161732973hg38UCSC Ensembl
Innerchr1:161691433..161702763hg19UCSC Ensembl
Innerchr1:159958057..159969387hg18UCSC Ensembl
Innerchr1:158423091..158434421hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3811331
hg1911331
hg1811331
hg1711331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679635, nssv670750
Samples
Known GenesFCRLB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516773
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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