A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11160760



Internal ID4194413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138463169..138466975hg38UCSC Ensembl
Innerchr3:138463178..138466967hg38UCSC Ensembl
Outerchr3:138463161..138466984hg38UCSC Ensembl
chr3:138182011..138185817hg19UCSC Ensembl
Innerchr3:138182020..138185809hg19UCSC Ensembl
Outerchr3:138182003..138185826hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597914
Supporting Variants
SamplesHG03782
Known GenesESYT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11160760
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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