A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018502



Internal ID21927845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90817731..90822454hg38UCSC Ensembl
chr5:90113548..90118271hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg384724
hg194724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557284
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018502
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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