A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453966



Internal ID232075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26004147..26004278hg38UCSC Ensembl
chr6:26004375..26004506hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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