A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698611



Internal ID15088577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31370751..31372782hg38UCSC Ensembl
Innerchr6:31338528..31340559hg19UCSC Ensembl
Innerchr6:31446507..31448538hg18UCSC Ensembl
Innerchr6:31446507..31448538hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg382032
hg192032
hg182032
hg172032
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698611
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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