A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603039



Internal ID6990071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166237023..166260500hg38UCSC Ensembl
Innerchr4:166237023..166260500hg38UCSC Ensembl
Outerchr4:166236523..166261000hg38UCSC Ensembl
chr4:167158175..167181652hg19UCSC Ensembl
Innerchr4:167158175..167181652hg19UCSC Ensembl
Outerchr4:167157675..167182152hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3823478
hg1923478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11682586, essv11682587, essv11682585
SamplesNA07347, HG01510, HG01777
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603039
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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