A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782729



Internal ID18823424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22030921..22385282hg38UCSC Ensembl
Innerchr14:22499160..22853685hg19UCSC Ensembl
Innerchr14:21569000..21923525hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38354362
hg19354526
hg18354526
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892469
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=163
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782729
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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