A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688802



Internal ID15078768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13755991..13796116hg38UCSC Ensembl
Innerchr8:13613500..13653625hg19UCSC Ensembl
Innerchr8:13657871..13697996hg18UCSC Ensembl
Innerchr8:13657871..13697996hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3840126
hg1940126
hg1840126
hg1740126
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)nssv688802
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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