A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587442



Internal ID16028165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34888938..34898861hg38UCSC Ensembl
Innerchr21:36261235..36271158hg19UCSC Ensembl
Innerchr21:35183105..35193028hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg389924
hg199924
hg189924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946734
Samples
Known GenesRUNX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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