A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603041



Internal ID6990073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166307587..166316458hg38UCSC Ensembl
Innerchr4:166308087..166315958hg38UCSC Ensembl
Outerchr4:166306587..166317458hg38UCSC Ensembl
chr4:167228739..167237610hg19UCSC Ensembl
Innerchr4:167229239..167237110hg19UCSC Ensembl
Outerchr4:167227739..167238610hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg388872
hg198872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11682589
SamplesHG01869
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603041
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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