A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008363



Internal ID21917706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175958007..176106667hg38UCSC Ensembl
chr5:175385010..175533670hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38148661
hg19148661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576806
Samples
Known GenesFAM153B, LOC100996385, THOC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008363
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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