A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327925



Internal ID22137967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76109077..76158474hg38UCSC Ensembl
chr6:76818794..76868191hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3849398
hg1949398
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3233269
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327925
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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