A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14290049



Internal ID22193333
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232026
Supporting Variants
SamplesHG00731
Known GenesGNAL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14290049
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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