A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796932



Internal ID18832377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9943026..10036488hg38UCSC Ensembl
Innerchr4:9944650..10038112hg19UCSC Ensembl
Innerchr4:9553748..9647210hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3893463
hg1993463
hg1893463
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893873
Supporting Variants
Samples
Known GenesSLC2A9
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796932
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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