A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894018



Internal ID19184872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120611403..120686461hg38UCSC Ensembl
Outerchr4:120611403..120686461hg38UCSC Ensembl
Innerchr4:121532558..121607616hg19UCSC Ensembl
Outerchr4:121532558..121607616hg19UCSC Ensembl
Innerchr4:121752008..121827066hg18UCSC Ensembl
Outerchr4:121752008..121827066hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3875059
hg1975059
hg1875059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779651
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894018
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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