A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462788



Internal ID240710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109165470..109165544hg38UCSC Ensembl
chr6:109486673..109486747hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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