A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193230



Internal ID20760270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67989891..68001955hg38UCSC Ensembl
chr17:65986007..65998071hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3812065
hg1912065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528999
Supporting Variants
Samples
Known GenesC17orf58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193230
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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