A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593117



Internal ID21785160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68630186..68630186hg38UCSC Ensembl
chr9:71245102..71245102hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593117
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