A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941570



Internal ID15888840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54037814..54041462hg38UCSC Ensembl
Innerchr20:52654353..52658001hg19UCSC Ensembl
Innerchr20:52087760..52091408hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg383649
hg193649
hg183649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586279
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)nssv941570
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