A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2899767



Internal ID15260213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47449930..47450486hg38UCSC Ensembl
Innerchr3:47491420..47491976hg19UCSC Ensembl
Innerchr3:47466424..47466980hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38557
hg19557
hg18557
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514150
Supporting Variants
SamplesNA10860
Known GenesSCAP
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2899767
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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