A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688256



Internal ID21210108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109357619..109357716hg38UCSC Ensembl
chr12:109795424..109795521hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688256
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.6875


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