A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587574



Internal ID16028297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41877778..41893574hg38UCSC Ensembl
Innerchr21:43297887..43313683hg19UCSC Ensembl
Innerchr21:42170956..42186752hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815797
hg1915797
hg1815797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947153
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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