A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515662



Internal ID15443273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149090068..149097583hg38UCSC Ensembl
Innerchr2:149946582..149954097hg19UCSC Ensembl
Innerchr2:149654828..149662343hg18UCSC Ensembl
Innerchr2:149772090..149779605hg17UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg387516
hg197516
hg187516
hg177516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664285, nssv670370, nssv674026, nssv659799
Samples
Known GenesLYPD6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515662
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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