A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946586



Internal ID15893856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26342944..26583066hg38UCSC Ensembl
Innerchr21:27715263..27955385hg19UCSC Ensembl
Innerchr21:26637134..26877256hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38240123
hg19240123
hg18240123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587335
Supporting Variants
Samples
Known GenesCYYR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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