A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087860



Internal ID21275854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38420491..38425281hg38UCSC Ensembl
Innerchr9:38420488..38425278hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg384791
hg194791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113258
Supporting Variants
Samplessample229
Known GenesIGFBPL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087860
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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