A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940985



Internal ID16234941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:50848416..50872643hg38UCSC Ensembl
Innerchr20:49464953..49489180hg19UCSC Ensembl
Innerchr20:48898360..48922587hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3824228
hg1924228
hg1824228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586179
Supporting Variants
Samples
Known GenesBCAS4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940985
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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