A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349051



Internal ID22192575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112138242..112138242hg38UCSC Ensembl
chr9:114900522..114900522hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565859
Supporting Variants
SamplesHG00731
Known GenesMIR3134, SUSD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349051
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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