A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701117



Internal ID124783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41322790..41325991hg38UCSC Ensembl
chr15:41614988..41618189hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505537
Supporting Variants
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701117
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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