A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041505



Internal ID21950838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36620788..36620856hg38UCSC Ensembl
chr20:35249191..35249259hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623312
Samples
Known GenesSLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041505
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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