A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349664



Internal ID22261726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97577143..97577143hg38UCSC Ensembl
chr9:100339425..100339425hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565557
Supporting Variants
SamplesNA19238
Known GenesTMOD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349664
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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