A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752127



Internal ID20527987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79564409..79564409hg38UCSC Ensembl
chr9:82179324..82179324hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752127
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer