A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634440



Internal ID21826487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33915609..33915609hg38UCSC Ensembl
chr18:31495573..31495573hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381588
hg191588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111248
Supporting Variants
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634440
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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