A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536452



Internal ID20909799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17969767..17972522hg38UCSC Ensembl
chr22:18452533..18455288hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg382756
hg192756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072861
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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