A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014105



Internal ID21923448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63976176..63976497hg38UCSC Ensembl
chrUn_gl000211:7739..8050hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38322
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014105
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