A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644519



Internal ID7031274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46052511..46064649hg38UCSC Ensembl
Innerchr19:46052511..46064649hg38UCSC Ensembl
Outerchr19:46052011..46065149hg38UCSC Ensembl
chr19:46555769..46567907hg19UCSC Ensembl
Innerchr19:46555769..46567907hg19UCSC Ensembl
Outerchr19:46555269..46568407hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3812139
hg1912139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16068462
SamplesNA19031
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644519
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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