A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701140



Internal ID124806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41573817..41577885hg38UCSC Ensembl
chr15:41866015..41870083hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384069
hg194069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511204
Supporting Variants
Samples
Known GenesTYRO3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.120478


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