A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457135



Internal ID22211633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175231430..175232801hg38UCSC Ensembl
chr1:175200566..175201937hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3545594
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14457135
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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