A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615097



Internal ID21807144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44794502..44794502hg38UCSC Ensembl
chr15:45086700..45086700hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615097
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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