A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933566



Internal ID21353635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49820974..49821502hg38UCSC Ensembl
chr14:50287692..50288220hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183330
SamplesHG002
Known GenesNEMF
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933566
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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