A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008930



Internal ID21918273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48775422..48776993hg38UCSC Ensembl
chr8:49687981..49689552hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381572
hg191572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008930
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