A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089773



Internal ID21282603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25873167..25876204hg38UCSC Ensembl
Innerchr10:26162096..26165133hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383038
hg193038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112230
Supporting Variants
Samplessample329
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089773
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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