A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937321



Internal ID15884591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2692558..2694089hg38UCSC Ensembl
Innerchr20:2673204..2674735hg19UCSC Ensembl
Innerchr20:2621204..2622735hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381532
hg191532
hg181532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585270
Supporting Variants
Samples
Known GenesEBF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937321
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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