A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717230



Internal ID140896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33928909..33928963hg38UCSC Ensembl
chr18:31508873..31508927hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145136
Supporting Variants
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717230
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005662


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