A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274060



Internal ID20483278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45941611..45941611hg38UCSC Ensembl
chr17:44018977..44018977hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755465
Supporting Variants
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274060
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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