A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761650



Internal ID20537510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10681783..10681783hg38UCSC Ensembl
chr5:10681895..10681895hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280105
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761650
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