A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507356



Internal ID284077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63672538..63677255hg38UCSC Ensembl
chr11:63440010..63444727hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384718
hg194718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507356
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