A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479716



Internal ID22537618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84131340..84147956hg38UCSC Ensembl
chr16:84164945..84181561hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3816617
hg1916617
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876860
Supporting Variants
Samples
Known GenesDNAAF1, HSDL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479716
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer