A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643631



Internal ID7030390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9254948..9262724hg38UCSC Ensembl
Innerchr19:9254998..9262674hg38UCSC Ensembl
Outerchr19:9254816..9262856hg38UCSC Ensembl
chr19:9365624..9373400hg19UCSC Ensembl
Innerchr19:9365674..9373350hg19UCSC Ensembl
Outerchr19:9365492..9373532hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387777
hg197777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990165
SamplesHG02983
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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