A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528572



Internal ID22397961
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385132, nssv14374943
SamplesHG00732, HG00733
Known GenesTTBK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528572
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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