A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600920



Internal ID6987959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69661584..69665436hg38UCSC Ensembl
Innerchr4:69661614..69665407hg38UCSC Ensembl
Outerchr4:69661555..69665466hg38UCSC Ensembl
chr4:70527302..70531154hg19UCSC Ensembl
Innerchr4:70527332..70531125hg19UCSC Ensembl
Outerchr4:70527273..70531184hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11493289, essv11493286, essv11493285, essv11493288, essv11493287
SamplesNA19066, HG03717, NA18988, NA19000, NA18953
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600920
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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