A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735273



Internal ID20511215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31636908..31637003hg38UCSC Ensembl
chr19:32127814..32127909hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735273
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