A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043689



Internal ID21952983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29442655..29457682hg38UCSC Ensembl
chr22:29838644..29853671hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3815028
hg1915028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043689
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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