A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401102



Internal ID22458972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25969826..25972005hg38UCSC Ensembl
chr22:26365792..26367971hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382180
hg192180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963620
Supporting Variants
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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