A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393136



Internal ID21050689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168467250..168469979hg38UCSC Ensembl
chr4:169388401..169391130hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115350
Samples
Known GenesDDX60L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393136
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