A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019861



Internal ID21929204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73919224..73919286hg38UCSC Ensembl
chr10:75678982..75679044hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582292
Samples
Known GenesC10orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019861
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