A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603481



Internal ID6990512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184972573..184987029hg38UCSC Ensembl
Innerchr4:184972584..184987018hg38UCSC Ensembl
Outerchr4:184972562..184987040hg38UCSC Ensembl
chr4:185893727..185908183hg19UCSC Ensembl
Innerchr4:185893738..185908172hg19UCSC Ensembl
Outerchr4:185893716..185908194hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814457
hg1914457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1050e214
Supporting Variantsessv11734394
SamplesNA19648
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603481
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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