A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191455



Internal ID20758495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83087765..83110212hg38UCSC Ensembl
chr17:81045641..81067162hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3822448
hg1921522
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522923
Supporting Variants
Samples
Known GenesMETRNL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00161


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