A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894076



Internal ID18838244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177303484..177340740hg38UCSC Ensembl
Outerchr4:177303484..177340740hg38UCSC Ensembl
Innerchr4:178224638..178261894hg19UCSC Ensembl
Outerchr4:178224638..178261894hg19UCSC Ensembl
Innerchr4:178461632..178498888hg18UCSC Ensembl
Outerchr4:178461632..178498888hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3837257
hg1937257
hg1837257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797233
Samples
Known GenesNEIL3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894076
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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