A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151375



Internal ID15508529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56694268..56769998hg38UCSC Ensembl
Innerchr20:55269324..55345054hg19UCSC Ensembl
Innerchr20:54702731..54778461hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3875731
hg1975731
hg1875731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586302
Supporting Variants
Samples1780862484_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151375
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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