A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586264



Internal ID16026987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031829..54038765hg38UCSC Ensembl
Innerchr20:52648368..52655304hg19UCSC Ensembl
Innerchr20:52081775..52088711hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386937
hg196937
hg186937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7607n54
Supporting Variantsnssv941528
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586264
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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