A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714721



Internal ID138387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76378386..76378386hg38UCSC Ensembl
chr17:74374467..74374467hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714721
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03824


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