A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459218



Internal ID237234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15310796..15331635hg38UCSC Ensembl
chr6:15311027..15331866hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3820840
hg1920840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979712
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459218
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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