A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019714



Internal ID21929057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11782763..11782889hg38UCSC Ensembl
chr8:11640272..11640398hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566628
Samples
Known GenesNEIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019714
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