A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073443



Internal ID21437651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124296754..124296754hg38UCSC Ensembl
chr11:124166650..124166650hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651647
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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