A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526355



Internal ID15106962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39751112..39752107hg38UCSC Ensembl
Innerchr8:39608631..39609626hg19UCSC Ensembl
Innerchr8:39727788..39728783hg18UCSC Ensembl
Innerchr8:39727788..39728783hg17UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38996
hg19996
hg18996
hg17996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702648
Samples
Known GenesADAM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526355
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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