A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382729



Internal ID22209727
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223177
Supporting Variants
SamplesHG00732
Known GenesTYRO3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382729
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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