A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894017



Internal ID19184871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120285335..120484900hg38UCSC Ensembl
Outerchr4:120278315..120484900hg38UCSC Ensembl
Innerchr4:121206490..121406055hg19UCSC Ensembl
Outerchr4:121199470..121406055hg19UCSC Ensembl
Innerchr4:121425940..121625505hg18UCSC Ensembl
Outerchr4:121418920..121625505hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38206586
hg19206586
hg18206586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782370, essv25783577, essv25796041
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894017
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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