A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504196



Internal ID281004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41559342..41561123hg38UCSC Ensembl
chr15:41851540..41853321hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381782
hg191782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701134
Samples
Known GenesTYRO3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504196
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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