A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941556



Internal ID15888826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54036316..54044202hg38UCSC Ensembl
Innerchr20:52652855..52660741hg19UCSC Ensembl
Innerchr20:52086262..52094148hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387887
hg197887
hg187887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586272
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)nssv941556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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