A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108141



Internal ID22017375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174819504..175487105hg38UCSC Ensembl
chr4:175740655..176408256hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38667602
hg19667602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542441
Samples
Known GenesADAM29, GLRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108141
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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