A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232026



Internal ID22372400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11817694..11825642hg38UCSC Ensembl
chr18:11817693..11825641hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg387949
hg197949
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290050, nssv14290049
SamplesHG00731, HG00733
Known GenesGNAL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232026
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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