A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937307



Internal ID15884577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2692558..2693630hg38UCSC Ensembl
Innerchr20:2673204..2674276hg19UCSC Ensembl
Innerchr20:2621204..2622276hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381073
hg191073
hg181073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585268
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)nssv937307
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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