A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090765



Internal ID21271626
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 StatusS
Merged Variantsnsv3112628
Supporting Variants
Samplessample166
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090765
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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