A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901082



Internal ID22676230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41946858..41946911hg38UCSC Ensembl
chr4:41948875..41948928hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421164
Samples
Known GenesTMEM33
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901082
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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