A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595763



Internal ID6983081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31944835..31947901hg38UCSC Ensembl
Innerchr3:31944885..31947851hg38UCSC Ensembl
Outerchr3:31944785..31947951hg38UCSC Ensembl
chr3:31986327..31989393hg19UCSC Ensembl
Innerchr3:31986377..31989343hg19UCSC Ensembl
Outerchr3:31986277..31989443hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg383067
hg193067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10972950
SamplesNA19917
Known GenesOSBPL10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595763
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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