A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14416398



Internal ID22152094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3232613..3293601hg38UCSC Ensembl
chr11:3253843..3314831hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3860989
hg1960989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224431
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)nssv14416398
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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