A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946618



Internal ID16240574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33281545..33285376hg38UCSC Ensembl
Innerchr21:34653850..34657681hg19UCSC Ensembl
Innerchr21:33575720..33579551hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383832
hg193832
hg183832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587377
Supporting Variants
Samples
Known GenesIL10RB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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