A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965286



Internal ID22740222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27014835..27014835hg38UCSC Ensembl
chr7:27054454..27054454hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965286
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