A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890239



Internal ID167651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9410185..9411549hg38UCSC Ensembl
chr1:9470244..9471608hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890239
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006246


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