A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147263



Internal ID346445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59538007..59543151hg38UCSC Ensembl
chr20:58113062..58118206hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg385145
hg195145
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147263
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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