A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477688



Internal ID22535589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24924653..24926024hg38UCSC Ensembl
chr16:24935974..24937345hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875814
Supporting Variants
Samples
Known GenesARHGAP17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477688
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