A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116592



Internal ID21299858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26319386..26510349hg38UCSC Ensembl
Innerchr6:26319614..26510577hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38190964
hg19190964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087604
Samplessample192
Known GenesBTN1A1, BTN2A1, BTN2A2, BTN2A3P, BTN3A1, BTN3A2, BTN3A3, LOC285819
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116592
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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