A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232339



Internal ID22372476
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320851
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232339
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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