A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615597



Internal ID21807644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89389149..89389149hg38UCSC Ensembl
chr15:89932380..89932380hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095897
Supporting Variants
Samples
Known GenesLINC00925
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615597
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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