A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326928



Internal ID22234481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27823835..27831816hg38UCSC Ensembl
chr6:27791613..27799594hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387982
hg197982
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3248059
Supporting Variants
SamplesHG00733
Known GenesHIST1H4J, HIST1H4K
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326928
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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