A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644223



Internal ID7030979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34907000..34908814hg38UCSC Ensembl
Innerchr19:34907000..34908814hg38UCSC Ensembl
Outerchr19:34906843..34908972hg38UCSC Ensembl
chr19:35397904..35399718hg19UCSC Ensembl
Innerchr19:35397904..35399718hg19UCSC Ensembl
Outerchr19:35397747..35399876hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381815
hg191815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16045261, essv16045262
SamplesHG02571, HG03270
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644223
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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