A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521614



Internal ID15448907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:222129805..222144299hg38UCSC Ensembl
Innerchr1:222303147..222317641hg19UCSC Ensembl
Innerchr1:220369770..220384264hg18UCSC Ensembl
Innerchr1:218691542..218706036hg17UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3814495
hg1914495
hg1814495
hg1714495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698232
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521614
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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