A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586977



Internal ID16374386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10515528..10599016hg38UCSC Ensembl
Innerchr21:10913441..10996929hg19UCSC Ensembl
Innerchr21:9935312..10018800hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3883489
hg1983489
hg1883489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944869
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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