A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700902



Internal ID124568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58484216..58485484hg38UCSC Ensembl
chr15:58776415..58777683hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524425
Supporting Variants
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.08382


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