A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046492



Internal ID21955731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50653501..50653655hg38UCSC Ensembl
chr20:49270038..49270192hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046492
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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