A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918718



Internal ID22693940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94701514..94721770hg38UCSC Ensembl
chr11:94434680..94454936hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3820257
hg1920257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918718
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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