A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455232



Internal ID22269900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62420001..62487139hg38UCSC Ensembl
chr9:46731302..46798440hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3867139
hg1967139
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3556728
Supporting Variants
SamplesNA19239
Known GenesKGFLP1
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455232
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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