A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521624



Internal ID15102231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119421736..119423465hg38UCSC Ensembl
Innerchr8:120433976..120435705hg19UCSC Ensembl
Innerchr8:120503157..120504886hg18UCSC Ensembl
Innerchr8:120503157..120504886hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381730
hg191730
hg181730
hg171730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698242
Samples
Known GenesNOV
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521624
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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