A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216492



Internal ID22362469
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 Variantsnssv14380949
SamplesHG00732
Known GenesTYRO3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216492
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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