A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095046



Internal ID21466935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45138988..45138988hg38UCSC Ensembl
chr15:45431186..45431186hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662451
Supporting Variants
SamplesHG03065
Known GenesDUOX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095046
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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