A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048027



Internal ID21957260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32628126..32629263hg38UCSC Ensembl
chr20:31215928..31217065hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048027
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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