A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050709



Internal ID21959942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33094297..33107032hg38UCSC Ensembl
chr20:31682103..31694838hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3812736
hg1912736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633700
Samples
Known GenesBPIFB4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050709
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