A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116314



Internal ID20683354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39600591..39602409hg38UCSC Ensembl
chr4:39602211..39604029hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381819
hg191819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383140
Supporting Variants
Samples
Known GenesSMIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116314
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