A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600022



Internal ID6987066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28638732..28735606hg38UCSC Ensembl
Innerchr4:28638734..28735604hg38UCSC Ensembl
Outerchr4:28638730..28735608hg38UCSC Ensembl
chr4:28640354..28737228hg19UCSC Ensembl
Innerchr4:28640356..28737226hg19UCSC Ensembl
Outerchr4:28640352..28737230hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3896875
hg1996875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11379159, essv11379160
SamplesNA18959, NA18956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600022
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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