A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461137



Internal ID22268209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168390177..168393080hg38UCSC Ensembl
chr6:168790857..168793760hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382904
hg192904
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3553591
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14461137
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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