A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526368



Internal ID15453661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141089148..141094845hg38UCSC Ensembl
Innerchr8:142099247..142104944hg19UCSC Ensembl
Innerchr8:142168429..142174126hg18UCSC Ensembl
Innerchr8:142168429..142174126hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg385698
hg195698
hg185698
hg175698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702663
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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