A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461652



Internal ID22299215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46372318..47419392hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381047075
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3544020
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14461652
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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