A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893893



Internal ID19184713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19483142..19627686hg38UCSC Ensembl
Outerchr4:19483142..19627686hg38UCSC Ensembl
Innerchr4:19484765..19629309hg19UCSC Ensembl
Outerchr4:19484765..19629309hg19UCSC Ensembl
Innerchr4:19093863..19238407hg18UCSC Ensembl
Outerchr4:19093863..19238407hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38144545
hg19144545
hg18144545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796590
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893893
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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