A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523915



Internal ID21848274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226224734..226234991hg38UCSC Ensembl
chr1:226412435..226422692hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3810258
hg1910258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982667
Supporting Variants
Samples
Known GenesLIN9, MIXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523915
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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