A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892528



Internal ID19183348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43012874..43061086hg38UCSC Ensembl
Outerchr14:43012874..43061086hg38UCSC Ensembl
Innerchr14:43482077..43530289hg19UCSC Ensembl
Outerchr14:43482077..43530289hg19UCSC Ensembl
Innerchr14:42551827..42600039hg18UCSC Ensembl
Outerchr14:42551827..42600039hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3848213
hg1948213
hg1848213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792483
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892528
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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