A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016576



Internal ID21925919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129508532..129512841hg38UCSC Ensembl
chr9:132270811..132275120hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384310
hg194310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586424
Samples
Known GenesLINC00963
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016576
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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