A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500200



Internal ID20873425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2851497..2855349hg38UCSC Ensembl
chr16:2901498..2905350hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190294
Samples
Known GenesPRSS22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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