A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048455



Internal ID21957688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63477407..63477558hg38UCSC Ensembl
chr20:62108760..62108911hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048455
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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