A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939189



Internal ID16233145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30195269..30287844hg38UCSC Ensembl
Innerchr20:29429945..29522520hg19UCSC Ensembl
Innerchr20:28043606..28136181hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3892576
hg1992576
hg1892576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585867
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)nssv939189
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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