A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537792



Internal ID20911127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37902446..37907895hg38UCSC Ensembl
chr22:38298453..38303902hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385450
hg195450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073933
Samples
Known GenesMICALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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