A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115766



Internal ID21299032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72691684..72694341hg38UCSC Ensembl
Innerchr10:74451442..74454099hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090155
Samplessample141
Known GenesMCU
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115766
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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