A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657005



Internal ID15046971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36741697..36748417hg38UCSC Ensembl
Innerchr21:38113998..38120718hg19UCSC Ensembl
Innerchr21:37035868..37042588hg18UCSC Ensembl
Innerchr21:37035868..37042588hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg386721
hg196721
hg186721
hg176721
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519597
Supporting Variants
Samples
Known GenesSIM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657005
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer