A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491960



Internal ID269186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140248232..140252726hg38UCSC Ensembl
chr7:139948032..139952526hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384495
hg194495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491960
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