A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643768



Internal ID7030526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15310318..15314782hg38UCSC Ensembl
Innerchr19:15310341..15314760hg38UCSC Ensembl
Outerchr19:15310296..15314805hg38UCSC Ensembl
chr19:15421129..15425593hg19UCSC Ensembl
Innerchr19:15421152..15425571hg19UCSC Ensembl
Outerchr19:15421107..15425616hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384465
hg194465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15999970
SamplesHG03873
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643768
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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