A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099106



Internal ID21454186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50065214..50065273hg38UCSC Ensembl
chr13:50639350..50639409hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584624
Supporting Variants
SamplesHG02011
Known GenesDLEU2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099106
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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