A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049302



Internal ID21958535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33064596..33075363hg38UCSC Ensembl
chr20:31652402..31663169hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3810768
hg1910768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633894
Samples
Known GenesBPIFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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