A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540871



Internal ID315563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39057564..39069700hg38UCSC Ensembl
chr22:39453569..39465705hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3812137
hg1912137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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