A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511659



Internal ID22569611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133217241..133227029hg38UCSC Ensembl
chr9:136092628..136102416hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg389789
hg199789
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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