A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715464



Internal ID139130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65620733..65620773hg38UCSC Ensembl
chr17:63616851..63616891hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715464
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.017885


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