A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346068



Internal ID22270112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60829684..60914499hg38UCSC Ensembl
chr9:41415956..41500771hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3884816
hg1984816
Variant TypeCNV duplication
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223706
Supporting Variants
SamplesNA19239
Known GenesSPATA31A5, SPATA31A7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346068
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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