A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465386



Internal ID243249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91879634..91883713hg38UCSC Ensembl
chr6:92589352..92593431hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384080
hg194080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465386
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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