A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045083



Internal ID21954353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37379922..37379982hg38UCSC Ensembl
chr20:36008325..36008385hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636296
Samples
Known GenesSRC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045083
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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