A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073451



Internal ID21452417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124489641..124489641hg38UCSC Ensembl
chr11:124359537..124359537hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652784
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073451
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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