A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695655



Internal ID15085621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94253949..94254040hg38UCSC Ensembl
Innerchr6:94963667..94963758hg19UCSC Ensembl
Innerchr6:95020388..95020479hg18UCSC Ensembl
Innerchr6:95020388..95020479hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3892
hg1992
hg1892
hg1792
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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