A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703551



Internal ID15440203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30993595..31006158hg38UCSC Ensembl
Innerchr21:32365914..32378477hg19UCSC Ensembl
Innerchr21:31287785..31300348hg18UCSC Ensembl
Innerchr21:31287785..31300348hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3812564
hg1912564
hg1812564
hg1712564
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527158
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703551
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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