A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643787



Internal ID7030545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15998820..16006529hg38UCSC Ensembl
Innerchr19:15998832..16006517hg38UCSC Ensembl
Outerchr19:15998808..16006541hg38UCSC Ensembl
chr19:16109630..16117339hg19UCSC Ensembl
Innerchr19:16109642..16117327hg19UCSC Ensembl
Outerchr19:16109618..16117351hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387710
hg197710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002708
SamplesHG02715
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643787
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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