A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512568



Internal ID22570522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27203425..27205724hg38UCSC Ensembl
chr9:27203423..27205722hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865412
Supporting Variants
Samples
Known GenesTEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512568
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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