A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146509



Internal ID345714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26300953..26301120hg38UCSC Ensembl
chr22:26696919..26697086hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728192
Samples
Known GenesSEZ6L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146509
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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