A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346946



Internal ID22185170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70037916..70038266hg38UCSC Ensembl
chr9:72652832..72653182hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224773
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346946
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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