A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697833



Internal ID15087799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:16195077..16239548hg38UCSC Ensembl
Innerchr6:16195308..16239779hg19UCSC Ensembl
Innerchr6:16303287..16347758hg18UCSC Ensembl
Innerchr6:16303287..16347758hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3844472
hg1944472
hg1844472
hg1744472
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521185
Supporting Variants
Samples
Known GenesGMPR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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