A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741027



Internal ID20517004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144413109..144413171hg38UCSC Ensembl
chr8:145638493..145638555hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285517
Samples
Known GenesSLC39A4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741027
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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