A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556412



Internal ID329549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:58513656..58513662hg38UCSC Ensembl
chr12:58907439..58907445hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17058817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556412
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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