A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608262



Internal ID21800309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92207272..92207272hg38UCSC Ensembl
chr15:92750502..92750502hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608262
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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