A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634104



Internal ID21826151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6544366..6544366hg38UCSC Ensembl
chr18:6544365..6544365hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102811
Supporting Variants
Samples
Known GenesC18orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634104
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