A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741640



Internal ID20517617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255302..133255509hg38UCSC Ensembl
chr9:136130689..136130896hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264084
Samples
Known GenesABO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741640
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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