A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948449



Internal ID16242405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45022032..45028691hg38UCSC Ensembl
Innerchr21:46441947..46448606hg19UCSC Ensembl
Innerchr21:45266375..45273034hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg386660
hg196660
hg186660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587827
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)nssv948449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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