A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113837



Internal ID21297103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51328090..51334641hg38UCSC Ensembl
Innerchr10:53087850..53094401hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg386552
hg196552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089031
Samplessample62
Known GenesPRKG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113837
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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