A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475373



Internal ID253011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54579746..54636765hg38UCSC Ensembl
chr7:54647439..54704458hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3857020
hg1957020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16995951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475373
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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