A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11189807



Internal ID5892210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153279523..153293625hg38UCSC Ensembl
chr3:152997312..153011414hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814103
hg1914103
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598221
Supporting Variants
SamplesNA19314
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11189807
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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