A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698239



Internal ID15434891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6114149..6129272hg38UCSC Ensembl
Innerchr6:6114382..6129505hg19UCSC Ensembl
Innerchr6:6059381..6074504hg18UCSC Ensembl
Innerchr6:6059381..6074504hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3815124
hg1915124
hg1815124
hg1715124
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521620
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698239
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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