A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538959



Internal ID20912266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25752595..25755316hg38UCSC Ensembl
chr22:26148562..26151283hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382722
hg192722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074157
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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