A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11023446



Internal ID3934118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59390082..59405750hg38UCSC Ensembl
Innerchr3:59390082..59405750hg38UCSC Ensembl
Outerchr3:59389582..59406250hg38UCSC Ensembl
chr3:59375808..59391476hg19UCSC Ensembl
Innerchr3:59375808..59391476hg19UCSC Ensembl
Outerchr3:59375308..59391976hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3815669
hg1915669
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596275
Supporting Variants
SamplesHG03585
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11023446
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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