A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476303



Internal ID253917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149095877..149096412hg38UCSC Ensembl
chr7:148792969..148793504hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476303
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