A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702368



Internal ID15439020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110101478..110132390hg38UCSC Ensembl
Innerchr8:111113707..111144619hg19UCSC Ensembl
Innerchr8:111182883..111213795hg18UCSC Ensembl
Innerchr8:111182883..111213795hg17UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3830913
hg1930913
hg1830913
hg1730913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526118
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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