A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357797



Internal ID22241780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71568878..71579777hg38UCSC Ensembl
chr11:71279924..71290823hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3233589
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357797
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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