A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903519



Internal ID905335
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595075
Supporting Variants
SamplesNA20903
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903519
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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