A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700291



Internal ID15436943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13776312..13794483hg38UCSC Ensembl
Innerchr21:15148633..15166804hg19UCSC Ensembl
Innerchr21:14070504..14088675hg18UCSC Ensembl
Innerchr21:14070504..14088675hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3818172
hg1918172
hg1818172
hg1718172
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515654
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700291
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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