A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11078853



Internal ID3174612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99027824..99085729hg38UCSC Ensembl
Innerchr3:99027827..99085727hg38UCSC Ensembl
Outerchr3:99027822..99085732hg38UCSC Ensembl
chr3:98746668..98804573hg19UCSC Ensembl
Innerchr3:98746671..98804571hg19UCSC Ensembl
Outerchr3:98746666..98804576hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3857906
hg1957906
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597126
Supporting Variants
SamplesHG02790
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11078853
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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