A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532898



Internal ID308808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14797664..14810912hg38UCSC Ensembl
chr19:14908476..14921724hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3813249
hg1913249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721728
Samples
Known GenesOR7C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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