A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599709



Internal ID6986754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13951869..13955594hg38UCSC Ensembl
Innerchr4:13951876..13955588hg38UCSC Ensembl
Outerchr4:13951863..13955601hg38UCSC Ensembl
chr4:13953493..13957218hg19UCSC Ensembl
Innerchr4:13953500..13957212hg19UCSC Ensembl
Outerchr4:13953487..13957225hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg383726
hg193726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11359374
SamplesNA18950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599709
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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