A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609140



Internal ID21801187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86857788..86857788hg38UCSC Ensembl
chr15:87401019..87401019hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100242
Supporting Variants
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609140
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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