A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939048



Internal ID16233004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26290557..26337643hg38UCSC Ensembl
Innerchr20:26271193..26318279hg19UCSC Ensembl
Innerchr20:26219193..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3847087
hg1947087
hg1847087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585801
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939048
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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