A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3249925



Internal ID22377405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34545248..34562456hg38UCSC Ensembl
chr14:35014454..35031662hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3817209
hg1917209
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463509, nssv14463285, nssv14465915, nssv14465839
SamplesNA19238, HG00731, HG00732, HG00733
Known GenesSNX6
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3249925
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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