A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151376



Internal ID15854821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56833797..56851305hg38UCSC Ensembl
Innerchr20:55408853..55426361hg19UCSC Ensembl
Innerchr20:54842260..54859768hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3817509
hg1917509
hg1817509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586308
Supporting Variants
Samples1780862345_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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