A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259367



Internal ID20468585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73833618..73833712hg38UCSC Ensembl
chr3:73882769..73882863hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259367
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