A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597962



Internal ID6985099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140767118..140779170hg38UCSC Ensembl
Innerchr3:140767618..140778670hg38UCSC Ensembl
Outerchr3:140766118..140780170hg38UCSC Ensembl
chr3:140485960..140498012hg19UCSC Ensembl
Innerchr3:140486460..140497512hg19UCSC Ensembl
Outerchr3:140484960..140499012hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3812053
hg1912053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11161232
SamplesHG03642
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597962
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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