A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701383



Internal ID125049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55733089..55774707hg38UCSC Ensembl
chr15:56025287..56066905hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3841619
hg1941619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522317
Supporting Variants
Samples
Known GenesPRTG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701383
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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