A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596958



Internal ID6637228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89422435..89423028hg38UCSC Ensembl
Innerchr3:89422485..89422978hg38UCSC Ensembl
Outerchr3:89422385..89423078hg38UCSC Ensembl
chr3:89471585..89472178hg19UCSC Ensembl
Innerchr3:89471635..89472128hg19UCSC Ensembl
Outerchr3:89471535..89472228hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11068928
SamplesNA19043
Known GenesEPHA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596958
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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