A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074840



Internal ID5127047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98421929..98432680hg38UCSC Ensembl
Innerchr3:98421961..98432649hg38UCSC Ensembl
Outerchr3:98421898..98432712hg38UCSC Ensembl
chr3:98140773..98151524hg19UCSC Ensembl
Innerchr3:98140805..98151493hg19UCSC Ensembl
Outerchr3:98140742..98151556hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810752
hg1910752
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597115
Supporting Variants
SamplesNA18565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074840
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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