A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15990265



Internal ID5021535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9938004..9938946hg38UCSC Ensembl
Innerchr19:9938054..9938896hg38UCSC Ensembl
Outerchr19:9937752..9939198hg38UCSC Ensembl
chr19:10048680..10049622hg19UCSC Ensembl
Innerchr19:10048730..10049572hg19UCSC Ensembl
Outerchr19:10048428..10049874hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643645
Supporting Variants
SamplesNA18516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15990265
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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