A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554095



Internal ID20927204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18024101..18024800hg38UCSC Ensembl
chr22:18506867..18507566hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072863
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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