A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604103



Internal ID21796150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24633403..24633403hg38UCSC Ensembl
chr14:25102609..25102609hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096521
Supporting Variants
Samples
Known GenesGZMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604103
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