A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586543



Internal ID16373952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63130372..63135463hg38UCSC Ensembl
Innerchr20:61761724..61766815hg19UCSC Ensembl
Innerchr20:61232169..61237260hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385092
hg195092
hg185092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7660n54
Supporting Variantsnssv943663, nssv943659, nssv943660, nssv943661, nssv943662
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586543
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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