A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010593



Internal ID21919936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115063966..115064084hg38UCSC Ensembl
chr8:116076195..116076313hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010593
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