A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv949278



Internal ID16243234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45969344..45978497hg38UCSC Ensembl
Innerchr21:47389258..47398411hg19UCSC Ensembl
Innerchr21:46213686..46222839hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg389154
hg199154
hg189154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587929
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)nssv949278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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