A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116109



Internal ID20683149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21784339..21821304hg38UCSC Ensembl
chr4:21785962..21822927hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3836966
hg1936966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366665
Supporting Variants
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116109
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