A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332385



Internal ID22253062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168692356..168695795hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383440
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232286
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332385
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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