A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586250



Internal ID16026973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031284..54054593hg38UCSC Ensembl
Innerchr20:52647823..52671132hg19UCSC Ensembl
Innerchr20:52081230..52104539hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3823310
hg1923310
hg1823310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941467
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586250
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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