A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072792



Internal ID21490091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126138084..126138084hg38UCSC Ensembl
chr11:126007979..126007979hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644634
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072792
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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