A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892554



Internal ID19183374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62185502..62244147hg38UCSC Ensembl
Outerchr14:62180723..62252165hg38UCSC Ensembl
Innerchr14:62652220..62710865hg19UCSC Ensembl
Outerchr14:62647441..62718883hg19UCSC Ensembl
Innerchr14:61721973..61780618hg18UCSC Ensembl
Outerchr14:61717194..61788636hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3871443
hg1971443
hg1871443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801630, essv25780569
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892554
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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