A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184341



Internal ID20751381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19185265..19195620hg38UCSC Ensembl
chr16:19196587..19206942hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3810356
hg1910356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515314
Supporting Variants
Samples
Known GenesSYT17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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