A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021694



Internal ID21931037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2801973..2802026hg38UCSC Ensembl
chr16:2851974..2852027hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606488
Samples
Known GenesPRSS41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021694
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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