A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475701



Internal ID22533599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11772200..11773856hg38UCSC Ensembl
chr16:11866056..11867712hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381657
hg191657
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869655
Supporting Variants
Samples
Known GenesZC3H7A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475701
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