A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542905



Internal ID20916156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17843134..17853035hg38UCSC Ensembl
chr22:18325900..18335801hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg389902
hg199902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072857
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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