A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088467



Internal ID21281317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3045415..3056805hg38UCSC Ensembl
Innerchr9:3045415..3056805hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3811391
hg1911391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110707
Supporting Variants
Samplessample31
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088467
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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