A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786041



Internal ID19176477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35197464..35263163hg38UCSC Ensembl
Innerchr14:35666670..35732369hg19UCSC Ensembl
Innerchr14:34736421..34802120hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3865700
hg1965700
hg1865700
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892500
Supporting Variants
Samples
Known GenesKIAA0391
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786041
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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