A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372882



Internal ID22293336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130532514..130532595hg38UCSC Ensembl
chr11:130402409..130402490hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206159
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372882
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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