A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633057



Internal ID21825104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78182216..78182216hg38UCSC Ensembl
chr17:76178297..76178297hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087229
Supporting Variants
Samples
Known GenesTK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633057
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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