A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694141



Internal ID15430793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94624429..94626268hg38UCSC Ensembl
Innerchr8:95636657..95638496hg19UCSC Ensembl
Innerchr8:95705833..95707672hg18UCSC Ensembl
Innerchr8:95705833..95707672hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381840
hg191840
hg181840
hg171840
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516679
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694141
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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