A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701626



Internal ID15438278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105284492..105292180hg38UCSC Ensembl
Innerchr8:106296720..106304408hg19UCSC Ensembl
Innerchr8:106365896..106373584hg18UCSC Ensembl
Innerchr8:106365896..106373584hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg387689
hg197689
hg187689
hg177689
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525494
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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