A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2854907



Internal ID15423171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:207573328..207576000hg38UCSC Ensembl
Innerchr1:207746673..207749345hg19UCSC Ensembl
Innerchr1:205813296..205815968hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382673
hg192673
hg182673
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514919
Supporting Variants
SamplesNA19239
Known GenesCR1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2854907
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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