A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599697



Internal ID6986742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13173985..13174825hg38UCSC Ensembl
Innerchr4:13173996..13174814hg38UCSC Ensembl
Outerchr4:13173974..13174836hg38UCSC Ensembl
chr4:13175609..13176449hg19UCSC Ensembl
Innerchr4:13175620..13176438hg19UCSC Ensembl
Outerchr4:13175598..13176460hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11359152
SamplesNA20581
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599697
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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