A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191509



Internal ID20758549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68540399..68565800hg38UCSC Ensembl
chr17:66536540..66561941hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3825402
hg1925402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534498
Supporting Variants
Samples
Known GenesFAM20A, PRKAR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191509
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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