A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995786



Internal ID21905129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165081465..165083894hg38UCSC Ensembl
chr4:166002617..166005046hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382430
hg192430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541707
Samples
Known GenesTMEM192
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995786
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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