A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643418



Internal ID7030181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2090782..2093259hg38UCSC Ensembl
Innerchr19:2090782..2093259hg38UCSC Ensembl
Outerchr19:2090479..2093564hg38UCSC Ensembl
chr19:2090781..2093258hg19UCSC Ensembl
Innerchr19:2090781..2093258hg19UCSC Ensembl
Outerchr19:2090478..2093563hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382478
hg192478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15968885, essv15968886
SamplesNA18595, HG02032
Known GenesMOB3A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643418
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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