A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357486



Internal ID21015039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4544001..4552800hg38UCSC Ensembl
chr4:4545728..4554527hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117670
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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