A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346485



Internal ID22132672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36474249..36475082hg38UCSC Ensembl
chr9:36474246..36475079hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528770
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346485
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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