A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346936



Internal ID22199439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69839584..69839958hg38UCSC Ensembl
chr9:72454500..72454874hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527469
Supporting Variants
SamplesHG00732
Known GenesC9orf135
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346936
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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