A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074797



Internal ID3756382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98134309..98166171hg38UCSC Ensembl
Innerchr3:98134309..98166171hg38UCSC Ensembl
Outerchr3:98133809..98166671hg38UCSC Ensembl
chr3:97853153..97885015hg19UCSC Ensembl
Innerchr3:97853153..97885015hg19UCSC Ensembl
Outerchr3:97852653..97885515hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3831863
hg1931863
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597108
Supporting Variants
SamplesHG03385
Known GenesOR5H14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074797
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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