A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457717



Internal ID22251717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:21836222..22618492hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38782271
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3556036
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14457717
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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