A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223177



Internal ID22367028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41573815..41577885hg38UCSC Ensembl
chr15:41866013..41870083hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14382729
SamplesHG00732
Known GenesTYRO3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223177
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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