A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073216



Internal ID21469568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14879524..14879639hg38UCSC Ensembl
chr11:14901070..14901185hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593132
Supporting Variants
SamplesHG03125
Known GenesCYP2R1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073216
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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