A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088844



Internal ID21287423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13571254..13575490hg38UCSC Ensembl
Innerchr9:13571253..13575489hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384237
hg194237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112410
Supporting Variants
Samplessample400
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088844
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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