A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461504



Internal ID239453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27238405..27247702hg38UCSC Ensembl
chr6:27206184..27215481hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg389298
hg199298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461504
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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