A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700160



Internal ID15090126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:92652391..92660248hg38UCSC Ensembl
Innerchr8:93664619..93672476hg19UCSC Ensembl
Innerchr8:93733795..93741652hg18UCSC Ensembl
Innerchr8:93733795..93741652hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387858
hg197858
hg187858
hg177858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524263
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700160
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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