A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072162



Internal ID21485753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102642291..102642291hg38UCSC Ensembl
chr11:102513022..102513022hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662233
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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