A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371540



Internal ID21029093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132603801..132991800hg38UCSC Ensembl
chr3:132322645..132710644hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38388000
hg19388000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094181
Samples
Known GenesACAD11, NPHP3, NPHP3-ACAD11, NPHP3-AS1, UBA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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