A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499806



Internal ID276761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47769649..47769714hg38UCSC Ensembl
chr12:48163432..48163497hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17056845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499806
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