A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14401882



Internal ID22304019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66146688..66147036hg38UCSC Ensembl
chr13:66720820..66721168hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221152
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)nssv14401882
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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