A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110634



Internal ID21293900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45139789..45144847hg38UCSC Ensembl
Innerchr22:45535670..45540728hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv737n145
Supporting Variantsnssv14102774
Samplessample111
Known GenesLOC100506714
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110634
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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