A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075804



Internal ID21457811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69837011..69837011hg38UCSC Ensembl
chr11:69651779..69651779hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652286
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075804
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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