A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073481



Internal ID21489629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128219467..128230507hg38UCSC Ensembl
chr11:128089362..128100402hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811041
hg1911041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596706
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073481
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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