A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523895



Internal ID15451188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128038548..128044866hg38UCSC Ensembl
Innerchr8:129050794..129057112hg19UCSC Ensembl
Innerchr8:129119976..129126294hg18UCSC Ensembl
Innerchr8:129119976..129126294hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg386319
hg196319
hg186319
hg176319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699738
Samples
Known GenesPVT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523895
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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