A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083079



Internal ID21508172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25206855..25207163hg38UCSC Ensembl
chr14:25676061..25676369hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584903
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083079
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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