A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11153437



Internal ID5953533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132229192..132231909hg38UCSC Ensembl
Innerchr3:132229242..132231859hg38UCSC Ensembl
Outerchr3:132229142..132231959hg38UCSC Ensembl
chr3:131948036..131950753hg19UCSC Ensembl
Innerchr3:131948086..131950703hg19UCSC Ensembl
Outerchr3:131947986..131950803hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382718
hg192718
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597819
Supporting Variants
SamplesNA19374
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11153437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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