A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479008



Internal ID256548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154702382..154712913hg38UCSC Ensembl
chr7:154494092..154504623hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3810532
hg1910532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005296
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479008
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