A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477687



Internal ID22535588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24905268..24906711hg38UCSC Ensembl
chr16:24916589..24918032hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381444
hg191444
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882076
Supporting Variants
Samples
Known GenesSLC5A11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477687
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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