A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715109



Internal ID138775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10000..67000hg38UCSC Ensembl
chr18:10001..67000hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3857001
hg1957000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527097
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715109
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008694


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