A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083086



Internal ID21284185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167008141..167033941hg38UCSC Ensembl
Innerchr6:167421629..167447429hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3825801
hg1925801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110943
Supporting Variants
Samplessample359
Known GenesFGFR1OP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083086
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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