A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529345



Internal ID22398737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29455174..29457356hg38UCSC Ensembl
chr17:27782192..27784374hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382183
hg192183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388418
SamplesNA19238
Known GenesTAOK1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529345
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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