A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11099841



Internal ID1101657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111073649..111077426hg38UCSC Ensembl
chr3:110792496..110796273hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383778
hg193778
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597384
Supporting Variants
SamplesHG01871
Known GenesPVRL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11099841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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