A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522716



Internal ID15103323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39665094..39737460hg38UCSC Ensembl
Innerchr8:39522613..39594979hg19UCSC Ensembl
Innerchr8:39641770..39714136hg18UCSC Ensembl
Innerchr8:39641770..39714136hg17UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3872367
hg1972367
hg1872367
hg1772367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698346
Samples
Known GenesADAM18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522716
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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