A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602839



Internal ID21794886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21858050..21858050hg38UCSC Ensembl
chr14:22326227..22326227hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602839
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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