A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473492



Internal ID22531385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8071580..8074958hg38UCSC Ensembl
chr16:8121582..8124960hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg383379
hg193379
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473492
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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