A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644339



Internal ID7031095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39960538..39961933hg38UCSC Ensembl
Innerchr19:39960538..39961933hg38UCSC Ensembl
Outerchr19:39960384..39962120hg38UCSC Ensembl
chr19:40466445..40467840hg19UCSC Ensembl
Innerchr19:40466445..40467840hg19UCSC Ensembl
Outerchr19:40466291..40468027hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381396
hg191396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16054647
SamplesNA19726
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644339
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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