A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746993



Internal ID20523009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2857054..2857240hg38UCSC Ensembl
chr16:2907055..2907241hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284038
Samples
Known GenesPRSS22
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746993
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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