A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268000



Internal ID20477218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36511607..36511671hg38UCSC Ensembl
chr14:36980812..36980876hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739636
Supporting Variants
Samples
Known GenesSFTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268000
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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