A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900846



Internal ID22675993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133015664..133061647hg38UCSC Ensembl
chr3:132734508..132780491hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3845984
hg1945984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405603
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900846
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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