A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643859



Internal ID7030616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19824168..19828006hg38UCSC Ensembl
Innerchr19:19824169..19828005hg38UCSC Ensembl
Outerchr19:19824167..19828007hg38UCSC Ensembl
chr19:19934977..19938815hg19UCSC Ensembl
Innerchr19:19934978..19938814hg19UCSC Ensembl
Outerchr19:19934976..19938816hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383839
hg193839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16006934, essv16006930, essv16006932, essv16006933, essv16006931, essv16006935
SamplesHG03950, NA19075, HG04162, HG04019, HG03974, HG04025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643859
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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