A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522913



Internal ID15450206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37486988..37496263hg38UCSC Ensembl
Innerchr8:37344506..37353781hg19UCSC Ensembl
Innerchr8:37463664..37472939hg18UCSC Ensembl
Innerchr8:37463664..37472939hg17UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg389276
hg199276
hg189276
hg179276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698573
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522913
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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