A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091217



Internal ID21432308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20506318..20506818hg38UCSC Ensembl
chr14:20974477..20974977hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598610
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091217
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