A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597368



Internal ID6984596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:110122867..110139563hg38UCSC Ensembl
Innerchr3:110122877..110139554hg38UCSC Ensembl
Outerchr3:110122858..110139573hg38UCSC Ensembl
chr3:109841714..109858410hg19UCSC Ensembl
Innerchr3:109841724..109858401hg19UCSC Ensembl
Outerchr3:109841705..109858420hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3816697
hg1916697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11098720, essv11098719
SamplesHG02573, HG01767
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597368
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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