A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587713



Internal ID16028436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43740172..43740914hg38UCSC Ensembl
Innerchr21:45160053..45160795hg19UCSC Ensembl
Innerchr21:43984481..43985223hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38743
hg19743
hg18743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7877n54
Supporting Variantsnssv948040, nssv948036, nssv948038, nssv948039, nssv948037
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587713
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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