A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941379



Internal ID15888649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031284..54039654hg38UCSC Ensembl
Innerchr20:52647823..52656193hg19UCSC Ensembl
Innerchr20:52081230..52089600hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg388371
hg198371
hg188371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586243
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer