A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978035



Internal ID22752970
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 StatusM
Merged Variants
Supporting Variantsnssv17359641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978035
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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