A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948020



Internal ID15895290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43739631..43740457hg38UCSC Ensembl
Innerchr21:45159512..45160338hg19UCSC Ensembl
Innerchr21:43983940..43984766hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38827
hg19827
hg18827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587704
Supporting Variants
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv948020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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