A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11094677



Internal ID2796393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106979648..107038592hg38UCSC Ensembl
Innerchr3:106979648..107038592hg38UCSC Ensembl
Outerchr3:106979148..107039092hg38UCSC Ensembl
chr3:106698495..106757439hg19UCSC Ensembl
Innerchr3:106698495..106757439hg19UCSC Ensembl
Outerchr3:106697995..106757939hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3858945
hg1958945
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597298
Supporting Variants
SamplesHG02470
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11094677
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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