A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600115



Internal ID6987159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32369637..32389163hg38UCSC Ensembl
Innerchr4:32369652..32389149hg38UCSC Ensembl
Outerchr4:32369623..32389178hg38UCSC Ensembl
chr4:32371259..32390785hg19UCSC Ensembl
Innerchr4:32371274..32390771hg19UCSC Ensembl
Outerchr4:32371245..32390800hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3819527
hg1919527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11388098
SamplesNA19095
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600115
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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