A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588330



Internal ID21780373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101910376..101910376hg38UCSC Ensembl
chr8:102922604..102922604hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061243
Supporting Variants
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588330
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