A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459689



Internal ID237699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89091774..89092947hg38UCSC Ensembl
chr6:89801493..89802666hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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