A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347263



Internal ID22120776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39471963..39477867hg38UCSC Ensembl
chr9:41616981..41622885hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385905
hg195905
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223165
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347263
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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