A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603023



Internal ID6990055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165667887..165672986hg38UCSC Ensembl
Innerchr4:165667902..165672972hg38UCSC Ensembl
Outerchr4:165667873..165673001hg38UCSC Ensembl
chr4:166589039..166594138hg19UCSC Ensembl
Innerchr4:166589054..166594124hg19UCSC Ensembl
Outerchr4:166589025..166594153hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11680911, essv11680910
SamplesNA21128, NA21104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603023
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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