A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948549



Internal ID15895819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45633539..45650804hg38UCSC Ensembl
Innerchr21:47053453..47070718hg19UCSC Ensembl
Innerchr21:45877881..45895146hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3817266
hg1917266
hg1817266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587864
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv948549
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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