A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595075



Internal ID6635350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3957444..4160335hg38UCSC Ensembl
Innerchr3:3957444..4160335hg38UCSC Ensembl
Outerchr3:3957300..4160446hg38UCSC Ensembl
chr3:3999128..4202019hg19UCSC Ensembl
Innerchr3:3999128..4202019hg19UCSC Ensembl
Outerchr3:3998984..4202130hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38202892
hg19202892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10903519, essv10903518
SamplesNA20903, HG04054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595075
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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