A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587699



Internal ID16028422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43551965..43555248hg38UCSC Ensembl
Innerchr21:44971846..44975129hg19UCSC Ensembl
Innerchr21:43796274..43799557hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383284
hg193284
hg183284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7873n54
Supporting Variantsnssv948015
Samples
Known GenesHSF2BP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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