A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704144



Internal ID15440796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87750691..87774549hg38UCSC Ensembl
Innerchr8:88762919..88786777hg19UCSC Ensembl
Innerchr8:88832035..88855893hg18UCSC Ensembl
Innerchr8:88832035..88855893hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3823859
hg1923859
hg1823859
hg1723859
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527669
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704144
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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