A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112027



Internal ID20679067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152491497..152492191hg38UCSC Ensembl
chr4:153412649..153413343hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382074
Supporting Variants
Samples
Known GenesFBXW7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112027
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