A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603366



Internal ID6990398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179881742..179901318hg38UCSC Ensembl
Innerchr4:179881892..179901168hg38UCSC Ensembl
Outerchr4:179881592..179901468hg38UCSC Ensembl
chr4:180802895..180822471hg19UCSC Ensembl
Innerchr4:180803045..180822321hg19UCSC Ensembl
Outerchr4:180802745..180822621hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3819577
hg1919577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1046e214
Supporting Variantsessv11727761
SamplesHG01392
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603366
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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