A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465839



Internal ID22218139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34545248..34562456hg38UCSC Ensembl
chr14:35014454..35031662hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3817209
hg1917209
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3249925
Supporting Variants
SamplesHG00733
Known GenesSNX6
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14465839
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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