A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14418826



Internal ID22155660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128868550..128868692hg38UCSC Ensembl
chr11:128738445..128738587hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218007
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14418826
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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