A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433103



Internal ID21395105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248576100..248634899hg38UCSC Ensembl
chr1:248739401..248798200hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3858800
hg1958800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv58n172
Supporting Variantsnssv15752659
SamplesMDQ025
Known GenesOR2T10, OR2T11
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433103
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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