A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375106



Internal ID22321610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67156795..67169738hg38UCSC Ensembl
chr11:66924266..66937209hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3812944
hg1912944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220318
Supporting Variants
SamplesNA19240
Known GenesKDM2A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375106
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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