A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892482



Internal ID19183302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26113646..26286465hg38UCSC Ensembl
Outerchr14:26113646..26286465hg38UCSC Ensembl
Innerchr14:26582852..26755671hg19UCSC Ensembl
Outerchr14:26582852..26755671hg19UCSC Ensembl
Innerchr14:25652692..25825511hg18UCSC Ensembl
Outerchr14:25652692..25825511hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38172820
hg19172820
hg18172820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25793049
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892482
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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