A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114634



Internal ID21297900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35257045..35259021hg38UCSC Ensembl
Innerchr22:35653038..35655014hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381977
hg191977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102847
Samplessample136
Known GenesHMGXB4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114634
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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