A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485268



Internal ID262663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149412354..149421858hg38UCSC Ensembl
chr7:149109445..149118949hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg389505
hg199505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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