A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247784



Internal ID22376799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60605282..60612178hg38UCSC Ensembl
chr14:61072000..61078896hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg386897
hg196897
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n152
Supporting Variantsnssv14370226, nssv14370225, nssv14370224
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247784
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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