A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151372



Internal ID15533823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031291..54036948hg38UCSC Ensembl
Innerchr20:52647830..52653487hg19UCSC Ensembl
Innerchr20:52081237..52086894hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg385658
hg195658
hg185658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586251
Supporting Variants
SamplesNINDS_220
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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