A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003402



Internal ID21912745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86047588..86101534hg38UCSC Ensembl
chr9:88662503..88716449hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3853947
hg1953947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578327
Samples
Known GenesGOLM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003402
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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