A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603387



Internal ID6990419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:180640126..180834655hg38UCSC Ensembl
Innerchr4:180640154..180834628hg38UCSC Ensembl
Outerchr4:180640099..180834683hg38UCSC Ensembl
chr4:181561279..181755808hg19UCSC Ensembl
Innerchr4:181561307..181755781hg19UCSC Ensembl
Outerchr4:181561252..181755836hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38194530
hg19194530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11728338
SamplesHG01678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603387
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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