A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936192



Internal ID22711543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9114211..9116665hg38UCSC Ensembl
chr19:9224887..9227341hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406445
Samples
Known GenesOR7G1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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