A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667480



Internal ID15057446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13757626..13799452hg38UCSC Ensembl
Innerchr8:13615135..13656961hg19UCSC Ensembl
Innerchr8:13659506..13701332hg18UCSC Ensembl
Innerchr8:13659506..13701332hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3841827
hg1941827
hg1841827
hg1741827
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)nssv667480
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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