A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109403



Internal ID20676443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133814188..133817037hg38UCSC Ensembl
chr4:134735343..134738192hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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