A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024062



Internal ID83753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64102000..64110960hg38UCSC Ensembl
chrUn_gl000211:133553..142513hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388961
hg198961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024062
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0292


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