A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075883



Internal ID21506970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75127393..75127393hg38UCSC Ensembl
chr11:74838438..74838438hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661279
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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