A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113919



Internal ID21297185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19532225..19537482hg38UCSC Ensembl
Innerchr6:19532456..19537713hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385258
hg195258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084546
Samplessample114
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113919
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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