A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349618



Internal ID22305001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95004706..95004758hg38UCSC Ensembl
chr9:97766988..97767040hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211116
Supporting Variants
SamplesNA19240
Known GenesC9orf3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349618
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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