A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006909



Internal ID21916252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86746407..86752775hg38UCSC Ensembl
chr5:86042224..86048592hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386369
hg196369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552350
Samples
Known GenesLOC100505878
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006909
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