A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996858



Internal ID20563898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113871301..113873000hg38UCSC Ensembl
chr12:114309106..114310805hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484948
Supporting Variants
Samples
Known GenesRBM19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02131


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