A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013572



Internal ID21922915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41651004..41651056hg38UCSC Ensembl
chr8:41508523..41508575hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013572
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