A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328367



Internal ID22285730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50225969..50347214hg38UCSC Ensembl
chr6:50193682..50314927hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38121246
hg19121246
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238295
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328367
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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