A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003221



Internal ID21912564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168633245..168657207hg38UCSC Ensembl
chr5:168060250..168084212hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3823963
hg1923963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003221
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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