A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091193



Internal ID21501677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99128277..99128396hg38UCSC Ensembl
chr14:99594614..99594733hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586966
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091193
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