A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973490



Internal ID22748425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93642422..93642422hg38UCSC Ensembl
chr11:93375588..93375588hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973490
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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