A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392585



Internal ID21383615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108221234..108221307hg38UCSC Ensembl
chr6:108542438..108542511hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703897
Samples
Known GenesSNX3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392585
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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