A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090364



Internal ID21432676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49820974..49821501hg38UCSC Ensembl
chr14:50287692..50288219hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604266
Supporting Variants
SamplesHG00731
Known GenesNEMF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090364
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