A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893752



Internal ID19184572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:101972970..102088748hg38UCSC Ensembl
Outerchr3:101972970..102088748hg38UCSC Ensembl
Innerchr3:101691814..101807592hg19UCSC Ensembl
Outerchr3:101691814..101807592hg19UCSC Ensembl
Innerchr3:103174504..103290282hg18UCSC Ensembl
Outerchr3:103174504..103290282hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38115779
hg19115779
hg18115779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790610
Samples
Known GenesLOC152225
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893752
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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