A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021845



Internal ID20588885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77442576..77444849hg38UCSC Ensembl
chr14:77908919..77911192hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489114
Supporting Variants
Samples
Known GenesVIPAS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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