A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477744



Internal ID22535645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29290217..29292934hg38UCSC Ensembl
chr16:29301538..29304255hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382718
hg192718
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477744
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