A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018732



Internal ID21928075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82139730..82140564hg38UCSC Ensembl
chr5:81435549..81436383hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551005
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018732
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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