A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479746



Internal ID22537648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88029435..88032787hg38UCSC Ensembl
chr16:88063041..88066393hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383353
hg193353
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870648
Supporting Variants
Samples
Known GenesBANP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479746
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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