A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599978



Internal ID6987022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26030610..26038435hg38UCSC Ensembl
Innerchr4:26030610..26038435hg38UCSC Ensembl
Outerchr4:26030473..26038598hg38UCSC Ensembl
chr4:26032232..26040057hg19UCSC Ensembl
Innerchr4:26032232..26040057hg19UCSC Ensembl
Outerchr4:26032095..26040220hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387826
hg197826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11373446, essv11373445, essv11373444, essv11373443, essv11373442
SamplesHG03687, HG03738, HG03866, HG03848, HG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599978
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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