A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217701



Internal ID22363275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89059325..89059438hg38UCSC Ensembl
chr9:91674240..91674353hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9653n152
Supporting Variantsnssv14348170, nssv14348171
SamplesNA19239, HG00514
Known GenesSHC3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217701
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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