A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465725



Internal ID243581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157022713..157032442hg38UCSC Ensembl
chr6:157343847..157353576hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg389730
hg199730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989790
Samples
Known GenesARID1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465725
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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