A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11443841



Internal ID3289035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57912116..57920141hg38UCSC Ensembl
Innerchr4:57912158..57920099hg38UCSC Ensembl
Outerchr4:57912074..57920183hg38UCSC Ensembl
chr4:58778282..58786307hg19UCSC Ensembl
Innerchr4:58778324..58786265hg19UCSC Ensembl
Outerchr4:58778240..58786349hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg388026
hg198026
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600611
Supporting Variants
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11443841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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