A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644874



Internal ID7031625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56678047..56680888hg38UCSC Ensembl
Innerchr19:56678197..56680738hg38UCSC Ensembl
Outerchr19:56677897..56681038hg38UCSC Ensembl
chr19:57189415..57192256hg19UCSC Ensembl
Innerchr19:57189565..57192106hg19UCSC Ensembl
Outerchr19:57189265..57192406hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382842
hg192842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16103299
SamplesHG04186
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644874
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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