A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479053



Internal ID22536955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67791241..67803298hg38UCSC Ensembl
chr16:67825144..67837201hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3812058
hg1912058
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881625
Supporting Variants
Samples
Known GenesRANBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479053
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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