A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475666



Internal ID22533564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10534199..10551455hg38UCSC Ensembl
chr16:10628056..10645312hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817257
hg1917257
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869242
Supporting Variants
Samples
Known GenesEMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475666
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