A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457760



Internal ID235797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108446325..108446604hg38UCSC Ensembl
chr6:108767528..108767807hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986720
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457760
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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