A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699137



Internal ID15435789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:24340533..24388541hg38UCSC Ensembl
Innerchr21:25712846..25760855hg19UCSC Ensembl
Innerchr21:24634717..24682726hg18UCSC Ensembl
Innerchr21:24634717..24682726hg17UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3848009
hg1948010
hg1848010
hg1748010
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523388
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699137
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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