A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956098



Internal ID22731290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41940046..41940046hg38UCSC Ensembl
chr4:41942063..41942063hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427153
Samples
Known GenesTMEM33
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956098
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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