A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459809



Internal ID22321921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5981170..5984654hg38UCSC Ensembl
chr17:5884490..5887974hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg383485
hg193485
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3550812
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459809
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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