A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737477



Internal ID20513438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137060301..137063459hg38UCSC Ensembl
chr3:136779143..136782301hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383159
hg193159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737477
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