A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549833



Internal ID323449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12698698..12699024hg38UCSC Ensembl
chrUn_gl000235:6968..7294hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549833
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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