A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112940



Internal ID21296206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99303024..99307674hg38UCSC Ensembl
Innerchr10:101062781..101067431hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384651
hg194651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv174n145
Supporting Variantsnssv14088528
Samplessample184
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112940
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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