A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347345



Internal ID22259995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40566552..40611534hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3844983
Variant TypeCNV duplication
Copy Number39
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218880
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347345
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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