A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459092



Internal ID237111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1441231..1441531hg38UCSC Ensembl
chr6:1441466..1441766hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459092
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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