A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102787



Internal ID21267715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27794958..27805943hg38UCSC Ensembl
Innerchr22:28190946..28201931hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3810986
hg1910986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112180
Supporting Variants
Samplessample116
Known GenesMN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102787
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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