A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561456



Internal ID18415846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10355790..10356121hg38UCSC Ensembl
Outerchr3:10355714..10356204hg38UCSC Ensembl
Innerchr3:10397474..10397805hg19UCSC Ensembl
Outerchr3:10397398..10397888hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv287e215
Supporting Variantsessv9760203
Samples
Known GenesATP2B2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561456
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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