A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118013



Internal ID21301279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25893585..25896483hg38UCSC Ensembl
Innerchr10:26182514..26185412hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382899
hg192899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089911
Samplessample402
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118013
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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