A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944812



Internal ID16238768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10526466..10741631hg38UCSC Ensembl
Innerchr21:10770826..10985991hg19UCSC Ensembl
Innerchr21:9792697..10007862hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38215166
hg19215166
hg18215166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586922
Supporting Variants
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv944812
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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