A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948042



Internal ID15895312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43740206..43740914hg38UCSC Ensembl
Innerchr21:45160087..45160795hg19UCSC Ensembl
Innerchr21:43984515..43985223hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587715
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)nssv948042
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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