A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3233738



Internal ID22372833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130525181..130535874hg38UCSC Ensembl
chr6:130846326..130857019hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg3810694
hg1910694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463315, nssv14466314, nssv14453880
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3233738
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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