A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010033



Internal ID21919376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168236950..168237008hg38UCSC Ensembl
chr5:167663955..167664013hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575405
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010033
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