A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476271



Internal ID22534169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14681722..14688491hg38UCSC Ensembl
chr16:14775579..14782348hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg386770
hg196770
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885189
Supporting Variants
Samples
Known GenesPLA2G10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476271
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