A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743786



Internal ID20519776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82908752..82908873hg38UCSC Ensembl
chr5:82204571..82204692hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743786
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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