A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087960



Internal ID21278601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13809779..13821054hg38UCSC Ensembl
Innerchr9:13809778..13821053hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3811276
hg1911276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116011
Supporting Variants
Samplessample271
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087960
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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