A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923903



Internal ID22699130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10942933..10964250hg38UCSC Ensembl
chr11:10964480..10985797hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3821318
hg1921318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923903
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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