A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997382



Internal ID20564422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11928449..11932476hg38UCSC Ensembl
chr12:12081383..12085410hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg384028
hg194028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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