A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512215



Internal ID22570167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20958499..20969149hg38UCSC Ensembl
chr9:20958498..20969148hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3810651
hg1910651
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861531
Supporting Variants
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512215
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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