A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055903



Internal ID105099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11779887..11801980hg38UCSC Ensembl
chr12:11932821..11954914hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3822094
hg1922094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507601
Supporting Variants
Samples
Known GenesETV6, RNU6-19P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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