A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347793



Internal ID22256113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83357214..83357277hg38UCSC Ensembl
chr9:85972129..85972192hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528510
Supporting Variants
SamplesNA19238
Known GenesFRMD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347793
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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