A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893674



Internal ID18837808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24049972..24107131hg38UCSC Ensembl
Outerchr3:24049972..24107131hg38UCSC Ensembl
Innerchr3:24091463..24148622hg19UCSC Ensembl
Outerchr3:24091463..24148622hg19UCSC Ensembl
Innerchr3:24066467..24123626hg18UCSC Ensembl
Outerchr3:24066467..24123626hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3857160
hg1957160
hg1857160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792981
Samples
Known GenesLINC00691
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893674
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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