A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551884



Internal ID325304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154909775..154909775hg38UCSC Ensembl
chr7:154701485..154701485hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384459
hg194459
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551884
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