A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115375



Internal ID20682415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169007578..169013605hg38UCSC Ensembl
chr4:169928729..169934756hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386028
hg196028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383188
Supporting Variants
Samples
Known GenesCBR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115375
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