A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479738



Internal ID22537640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86720556..86725685hg38UCSC Ensembl
chr16:86754162..86759291hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385130
hg195130
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479738
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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