A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586968



Internal ID16374377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10549490..10657385hg38UCSC Ensembl
Innerchr21:10855072..10962967hg19UCSC Ensembl
Innerchr21:9876943..9984838hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38107896
hg19107896
hg18107896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7748n54
Supporting Variantsnssv944860
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586968
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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