A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701376



Internal ID125042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55615982..55616036hg38UCSC Ensembl
chr15:55908180..55908234hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519013
Supporting Variants
Samples
Known GenesPRTG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701376
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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