A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586895



Internal ID16374304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10540506..10804226hg38UCSC Ensembl
Innerchr21:10708231..10971951hg19UCSC Ensembl
Innerchr21:9730102..9993822hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38263721
hg19263721
hg18263721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7731n54
Supporting Variantsnssv944784
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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