A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11038913



Internal ID6009723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73094083..73095940hg38UCSC Ensembl
Innerchr3:73094133..73095890hg38UCSC Ensembl
Outerchr3:73094033..73095990hg38UCSC Ensembl
chr3:73143234..73145091hg19UCSC Ensembl
Innerchr3:73143284..73145041hg19UCSC Ensembl
Outerchr3:73143184..73145141hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596552
Supporting Variants
SamplesNA19404
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11038913
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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