A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183662



Internal ID20750702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13571735..13589655hg38UCSC Ensembl
chr17:13475052..13492972hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3817921
hg1917921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503251
Supporting Variants
Samples
Known GenesHS3ST3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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