A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892476



Internal ID19183296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23840656..23858581hg38UCSC Ensembl
Outerchr14:23840656..23858581hg38UCSC Ensembl
Innerchr14:24309865..24327790hg19UCSC Ensembl
Outerchr14:24309865..24327790hg19UCSC Ensembl
Innerchr14:23379705..23397630hg18UCSC Ensembl
Outerchr14:23379705..23397630hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3817926
hg1917926
hg1817926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780632, essv25801380
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892476
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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