A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700819



Internal ID15090785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93771444..93872365hg38UCSC Ensembl
Innerchr6:94481162..94582083hg19UCSC Ensembl
Innerchr6:94537883..94638804hg18UCSC Ensembl
Innerchr6:94537883..94638804hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38100922
hg19100922
hg18100922
hg17100922
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known GenesTSG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700819
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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