A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110734



Internal ID21294000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45158685..45160665hg38UCSC Ensembl
Innerchr22:45554566..45556546hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103613, nssv14103005, nssv14102993, nssv14102682, nssv14103580
Samplessample60, sample266, sample170, sample274, sample155
Known GenesLOC100506714
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110734
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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