A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724601



Internal ID148267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48806595..48806646hg38UCSC Ensembl
chr17:46883957..46884008hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557233
Supporting Variants
Samples
Known GenesTTLL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724601
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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