A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2868519



Internal ID15767051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38213431..38213879hg38UCSC Ensembl
Innerchr22:38609438..38609886hg19UCSC Ensembl
Innerchr22:36939384..36939832hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38449
hg19449
hg18449
Variant TypeCNV gain
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514970
Supporting Variants
SamplesNA19223
Known GenesMAFF
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2868519
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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