A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940541



Internal ID21360610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107557222..107557323hg38UCSC Ensembl
chr5:106892923..106893024hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196710
SamplesHG002
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940541
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