A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029029



Internal ID20596069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2851524..2855300hg38UCSC Ensembl
chr16:2901525..2905301hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383777
hg193777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511866
Supporting Variants
Samples
Known GenesPRSS22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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