A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073044



Internal ID21412531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123310157..123310215hg38UCSC Ensembl
chr11:123180865..123180923hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585653
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073044
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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