A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756643



Internal ID20532503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127408225..127408225hg38UCSC Ensembl
chr9:130170504..130170504hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756643
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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