A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453880



Internal ID22253826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130525181..130535874hg38UCSC Ensembl
chr6:130846326..130857019hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg3810694
hg1910694
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3233738
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453880
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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