A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155554



Internal ID22086059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14790966..14812225hg38UCSC Ensembl
Outerchr19:14785405..14815522hg38UCSC Ensembl
Innerchr19:14901778..14923037hg19UCSC Ensembl
Outerchr19:14896217..14926334hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3830118
hg1930118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013455
Samples
Known GenesOR7C1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155554
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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