A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797160



Internal ID19167661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16183902..16232642hg38UCSC Ensembl
Innerchr4:16185525..16234265hg19UCSC Ensembl
Innerchr4:15794623..15843363hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3848741
hg1948741
hg1848741
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893887
Supporting Variants
Samples
Known GenesTAPT1, TAPT1-AS1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797160
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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