A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893887



Internal ID19184707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16183902..16232642hg38UCSC Ensembl
Outerchr4:16183902..16232642hg38UCSC Ensembl
Innerchr4:16185525..16234265hg19UCSC Ensembl
Outerchr4:16185525..16234265hg19UCSC Ensembl
Innerchr4:15794623..15843363hg18UCSC Ensembl
Outerchr4:15794623..15843363hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3848741
hg1948741
hg1848741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797160
Samples
Known GenesTAPT1, TAPT1-AS1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893887
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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