A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523192



Internal ID15103799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40658085..40681837hg38UCSC Ensembl
Innerchr8:40515604..40539356hg19UCSC Ensembl
Innerchr8:40634761..40658513hg18UCSC Ensembl
Innerchr8:40634761..40658513hg17UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3823753
hg1923753
hg1823753
hg1723753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698908
Samples
Known GenesZMAT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523192
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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