A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746249



Internal ID20522260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181742936..181743025hg38UCSC Ensembl
chr3:181460724..181460813hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746249
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