A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385132



Internal ID22237733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42801161..42801318hg38UCSC Ensembl
chr15:43093359..43093516hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528572
Supporting Variants
SamplesHG00733
Known GenesTTBK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385132
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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