A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347675



Internal ID22146566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123977744..123992370hg38UCSC Ensembl
chr9:126740023..126754649hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3814627
hg1914627
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3242008
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347675
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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