A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914842



Internal ID22690059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142753059..142774543hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3821485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1928n209
Supporting Variantsnssv17441673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914842
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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