A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892500



Internal ID19183320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35197464..35263163hg38UCSC Ensembl
Outerchr14:35197464..35263163hg38UCSC Ensembl
Innerchr14:35666670..35732369hg19UCSC Ensembl
Outerchr14:35666670..35732369hg19UCSC Ensembl
Innerchr14:34736421..34802120hg18UCSC Ensembl
Outerchr14:34736421..34802120hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3865700
hg1965700
hg1865700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786041
Samples
Known GenesKIAA0391
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892500
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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