A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623616



Internal ID21815663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2614564..2614564hg38UCSC Ensembl
chr18:2614563..2614563hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109808
Supporting Variants
Samples
Known GenesNDC80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623616
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