A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14320851



Internal ID22226889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50257182..50286056hg38UCSC Ensembl
chr5:49553016..49581890hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3828875
hg1928875
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232339
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14320851
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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