A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739902



Internal ID20515877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127408225..127408680hg38UCSC Ensembl
chr9:130170504..130170959hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739902
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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