A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586262



Internal ID16026985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031829..54036948hg38UCSC Ensembl
Innerchr20:52648368..52653487hg19UCSC Ensembl
Innerchr20:52081775..52086894hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg385120
hg195120
hg185120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7609n54
Supporting Variantsnssv1151373
Samples1782681216_A
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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