A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606416



Internal ID21798463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100276168..100276168hg38UCSC Ensembl
chr15:100816373..100816373hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085230
Supporting Variants
Samples
Known GenesADAMTS17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606416
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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