A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033636



Internal ID21942979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58994182..59004293hg38UCSC Ensembl
chr15:59286381..59296492hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg3810112
hg1910112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603334
Samples
Known GenesRNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033636
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