A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032051



Internal ID21941394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101892192..101896845hg38UCSC Ensembl
chr11:101762923..101767576hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg384654
hg194654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583110
Samples
Known GenesANGPTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032051
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