A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605056



Internal ID21797103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97641174..97641174hg38UCSC Ensembl
chr15:98184404..98184404hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605056
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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