A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799591



Internal ID19161277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85892223..86060422hg38UCSC Ensembl
Innerchr14:86358567..86526766hg19UCSC Ensembl
Innerchr14:85428320..85596519hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38168200
hg19168200
hg18168200
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892569
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799591
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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