A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246766



Internal ID22376522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604530..60613253hg38UCSC Ensembl
chr14:61071248..61079971hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388724
hg198724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n152
Supporting Variantsnssv14463821, nssv14457292, nssv14459327
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246766
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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