A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3325289



Internal ID14825570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62574321..62574340hg38UCSC Ensembl
Innerchr3:62574317..62574344hg38UCSC Ensembl
Outerchr3:62574298..62574363hg38UCSC Ensembl
chr3:62559996..62560015hg19UCSC Ensembl
Innerchr3:62559992..62560019hg19UCSC Ensembl
Outerchr3:62559973..62560038hg19UCSC Ensembl
chr3:62535036..62535055hg18UCSC Ensembl
Innerchr3:62535059..62535032hg18UCSC Ensembl
Outerchr3:62535013..62535078hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8678762
SamplesNA19240
Known GenesCADPS
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3325289
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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