A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703111



Internal ID15093077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94625294..94712156hg38UCSC Ensembl
Innerchr6:95335012..95421874hg19UCSC Ensembl
Innerchr6:95391733..95478595hg18UCSC Ensembl
Innerchr6:95391733..95478595hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3886863
hg1986863
hg1886863
hg1786863
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)nssv703111
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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