A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870169



Internal ID22645104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58294097..58295446hg38UCSC Ensembl
chr16:58328001..58329350hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472147
Samples
Known GenesPRSS54
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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