A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2854899



Internal ID15336606
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 loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514919
Supporting Variants
SamplesNA18594
Known GenesCR1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2854899
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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