A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643622



Internal ID7030381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8628906..8631151hg38UCSC Ensembl
Innerchr19:8628943..8631115hg38UCSC Ensembl
Outerchr19:8628870..8631188hg38UCSC Ensembl
chr19:8738356..8740601hg19UCSC Ensembl
Innerchr19:8738393..8740565hg19UCSC Ensembl
Outerchr19:8738320..8740638hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15989249, essv15989250
SamplesHG01859, HG00704
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643622
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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