A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039669



Internal ID21949012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2786675..2787459hg38UCSC Ensembl
chr16:2836676..2837460hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605998
Samples
Known GenesPRSS33
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039669
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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