A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291623



Internal ID20500841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92023775..92023775hg38UCSC Ensembl
chr15:92567005..92567005hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762217
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291623
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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