A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112628



Internal ID21295894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126144734..126149751hg38UCSC Ensembl
Innerchr9:128907013..128912030hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385018
hg195018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090765
Samplessample166
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112628
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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