A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242008



Internal ID22375137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123977744..123992370hg38UCSC Ensembl
chr9:126740023..126754649hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3814627
hg1914627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9742n152
Supporting Variantsnssv14347677, nssv14347675, nssv14347680, nssv14347674, nssv14347679, nssv14347678, nssv14347676
SamplesNA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242008
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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