A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937340



Internal ID15884610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2693073..2696059hg38UCSC Ensembl
Innerchr20:2673719..2676705hg19UCSC Ensembl
Innerchr20:2621719..2624705hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382987
hg192987
hg182987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585275
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)nssv937340
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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