A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587739



Internal ID16028462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44208491..44220746hg38UCSC Ensembl
Innerchr21:45628374..45640629hg19UCSC Ensembl
Innerchr21:44452802..44465057hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3812256
hg1912256
hg1812256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948222
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587739
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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