A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10979500



Internal ID2479046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34218571..34249432hg38UCSC Ensembl
Innerchr3:34218571..34249432hg38UCSC Ensembl
Outerchr3:34218071..34249932hg38UCSC Ensembl
chr3:34260063..34290924hg19UCSC Ensembl
Innerchr3:34260063..34290924hg19UCSC Ensembl
Outerchr3:34259563..34291424hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3830862
hg1930862
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595807
Supporting Variants
SamplesHG02184
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10979500
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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