A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388107



Internal ID22305405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11269889..11272076hg38UCSC Ensembl
chr11:11291436..11293623hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203738
Supporting Variants
SamplesNA19240
Known GenesGALNT18
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388107
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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