A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14464532



Internal ID22276681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40232818..40236154hg38UCSC Ensembl
chr4:40234438..40237774hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3552937
Supporting Variants
SamplesNA19239
Known GenesRHOH
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14464532
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer