A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11154832



Internal ID5722031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132878752..132879888hg38UCSC Ensembl
Innerchr3:132878752..132879888hg38UCSC Ensembl
Outerchr3:132878497..132880168hg38UCSC Ensembl
chr3:132597596..132598732hg19UCSC Ensembl
Innerchr3:132597596..132598732hg19UCSC Ensembl
Outerchr3:132597341..132599012hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597835
Supporting Variants
SamplesNA19099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11154832
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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