A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213433



Internal ID22360384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13501228..13501334hg38UCSC Ensembl
chr17:13404545..13404651hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384895
SamplesNA19238
Known GenesHS3ST3A1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213433
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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