A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702591



Internal ID126257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83492338..83492361hg38UCSC Ensembl
chr15:84161090..84161113hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550830
Supporting Variants
Samples
Known GenesSH3GL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702591
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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