A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463465



Internal ID22198197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46896485..46916160hg38UCSC Ensembl
chr12:47290268..47309943hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3819676
hg1919676
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231472
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14463465
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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