A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2889280



Internal ID15758667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100828498..100952002hg38UCSC Ensembl
Innerchr3:100547342..100670846hg19UCSC Ensembl
Innerchr3:102030032..102153536hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38123505
hg19123505
hg18123505
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514163
Supporting Variants
SamplesNA19194
Known GenesABI3BP
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2889280
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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