A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111295



Internal ID21294561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141822610..141916189hg38UCSC Ensembl
Innerchr6:142143747..142237326hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3893580
hg1993580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082820, nssv14083751
Samplessample6, sample73
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111295
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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