A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474822



Internal ID22532717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9111031..9139857hg38UCSC Ensembl
chr16:9204888..9233714hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3828827
hg1928827
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877632
Supporting Variants
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474822
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