A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536179



Internal ID20909534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24639175..24744988hg38UCSC Ensembl
chr22:25035142..25140955hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38105814
hg19105814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206772
Samples
Known GenesBCRP3, PIWIL3, POM121L10P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536179
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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