A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995940



Internal ID20562980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10498792..10499311hg38UCSC Ensembl
chr12:10651391..10651910hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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