A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087658



Internal ID21996891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2801971..2801971hg38UCSC Ensembl
chr16:2851972..2851972hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613116
Samples
Known GenesPRSS41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087658
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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