A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620490



Internal ID21812537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9269021..9269021hg38UCSC Ensembl
chr17:9172338..9172338hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089231
Supporting Variants
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620490
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