A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973810



Internal ID22748745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110930827..110930827hg38UCSC Ensembl
chr11:110801551..110801551hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973810
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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