A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037052



Internal ID21946395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66794979..66795066hg38UCSC Ensembl
chr11:66562450..66562537hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577713
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037052
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