A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462106



Internal ID240041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22886277..22887026hg38UCSC Ensembl
chr6:22886506..22887255hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462106
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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