A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798080



Internal ID19163269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67724729..67803187hg38UCSC Ensembl
Innerchr2:67951861..68030319hg19UCSC Ensembl
Innerchr2:67805365..67883823hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3878459
hg1978459
hg1878459
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892592
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=33
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798080
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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