A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903165



Internal ID22678330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102186328..102186423hg38UCSC Ensembl
chr3:101905172..101905267hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903165
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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