A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664071



Internal ID15054037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13819910..13834674hg38UCSC Ensembl
Innerchr8:13677419..13692183hg19UCSC Ensembl
Innerchr8:13721790..13736554hg18UCSC Ensembl
Innerchr8:13721790..13736554hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3814765
hg1914765
hg1814765
hg1714765
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664071
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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