A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007220



Internal ID21916563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22123885..22127180hg38UCSC Ensembl
chr10:22412814..22416109hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007220
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