A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111132



Internal ID21294398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124959988..124964373hg38UCSC Ensembl
Innerchr6:125281134..125285519hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384386
hg194386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086464
Samplessample149
Known GenesRNF217, STL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111132
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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