A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463787



Internal ID241678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164268086..164271155hg38UCSC Ensembl
chr6:164689119..164692188hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv440n206
Supporting Variantsnssv16990561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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