A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700904



Internal ID124570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58532950..58533106hg38UCSC Ensembl
chr15:58825149..58825305hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519951
Supporting Variants
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700904
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer