A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480452



Internal ID22538355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9818220..9819519hg38UCSC Ensembl
chr19:9928896..9930195hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878575
Supporting Variants
Samples
Known GenesFBXL12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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