A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892497



Internal ID19183317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31950125..31985304hg38UCSC Ensembl
Outerchr14:31950125..31985304hg38UCSC Ensembl
Innerchr14:32419331..32454510hg19UCSC Ensembl
Outerchr14:32419331..32454510hg19UCSC Ensembl
Innerchr14:31489082..31524261hg18UCSC Ensembl
Outerchr14:31489082..31524261hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3835180
hg1935180
hg1835180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790534
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892497
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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