A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523096



Internal ID15450389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102478686..102486560hg38UCSC Ensembl
Innerchr8:103490914..103498788hg19UCSC Ensembl
Innerchr8:103560090..103567964hg18UCSC Ensembl
Innerchr8:103560090..103567964hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg387875
hg197875
hg187875
hg177875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698788
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523096
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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