A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941238



Internal ID15888508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54030387..54038008hg38UCSC Ensembl
Innerchr20:52646926..52654547hg19UCSC Ensembl
Innerchr20:52080333..52087954hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387622
hg197622
hg187622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586233
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)nssv941238
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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