A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15990289



Internal ID5992105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10050592..10056925hg38UCSC Ensembl
Innerchr19:10050742..10056775hg38UCSC Ensembl
Outerchr19:10050442..10057075hg38UCSC Ensembl
chr19:10161268..10167601hg19UCSC Ensembl
Innerchr19:10161418..10167451hg19UCSC Ensembl
Outerchr19:10161118..10167751hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386334
hg196334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643647
Supporting Variants
SamplesHG02979
Known GenesC3P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15990289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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