A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10989676



Internal ID2206068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41028388..41031855hg38UCSC Ensembl
Innerchr3:41028388..41031855hg38UCSC Ensembl
Outerchr3:41028193..41032046hg38UCSC Ensembl
chr3:41069879..41073346hg19UCSC Ensembl
Innerchr3:41069879..41073346hg19UCSC Ensembl
Outerchr3:41069684..41073537hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383468
hg193468
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595962
Supporting Variants
SamplesHG01986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10989676
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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