A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918825



Internal ID22694047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63931434..63934471hg38UCSC Ensembl
chr11:63698906..63701943hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383038
hg193038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918825
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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