A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088415



Internal ID21267219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4590455..4597537hg38UCSC Ensembl
Innerchr9:4590455..4597537hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg387083
hg197083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114325
Supporting Variants
Samplessample11
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088415
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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