A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724826



Internal ID148492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56893223..56893223hg38UCSC Ensembl
chr17:54970584..54970584hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548560
Supporting Variants
Samples
Known GenesTRIM25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008926


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