A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386682



Internal ID22444552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25179975..25179975hg38UCSC Ensembl
chr16:25191296..25191296hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386682
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer