A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527164



Internal ID15107771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128460766..128682763hg38UCSC Ensembl
Innerchr8:129473012..129695009hg19UCSC Ensembl
Innerchr8:129542194..129764191hg18UCSC Ensembl
Innerchr8:129542194..129764191hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38221998
hg19221998
hg18221998
hg17221998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703558
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527164
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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