A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700688



Internal ID15437340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:116383534..116387659hg38UCSC Ensembl
Innerchr6:116704697..116708822hg19UCSC Ensembl
Innerchr6:116811390..116815515hg18UCSC Ensembl
Innerchr6:116811390..116815515hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg384126
hg194126
hg184126
hg174126
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524705
Supporting Variants
Samples
Known GenesDSE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700688
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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