A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056189



Internal ID21965422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15993955..15994109hg38UCSC Ensembl
chr20:15974600..15974754hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627974
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056189
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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