A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998674



Internal ID21908017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:941603..941681hg38UCSC Ensembl
chr4:935391..935469hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555877
Samples
Known GenesTMEM175
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998674
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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