A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596406



Internal ID6983721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64482618..64487955hg38UCSC Ensembl
Innerchr3:64482626..64487947hg38UCSC Ensembl
Outerchr3:64482610..64487963hg38UCSC Ensembl
chr3:64468294..64473631hg19UCSC Ensembl
Innerchr3:64468302..64473623hg19UCSC Ensembl
Outerchr3:64468286..64473639hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385338
hg195338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11029276
SamplesHG03917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596406
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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