A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472293



Internal ID22530185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68558422..68567321hg38UCSC Ensembl
chr16:68592325..68601224hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884619
Supporting Variants
Samples
Known GenesZFP90
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472293
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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