A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11680911



Internal ID6945836
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603023
Supporting Variants
SamplesNA21128
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11680911
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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