A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087877



Internal ID21276306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124958328..124968716hg38UCSC Ensembl
Innerchr9:127720607..127730995hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810389
hg1910389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110921
Supporting Variants
Samplessample234
Known GenesSCAI
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087877
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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