A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2846209



Internal ID15354002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109679679..109700311hg38UCSC Ensembl
Innerchr1:110222301..110242933hg19UCSC Ensembl
Innerchr1:110023824..110044456hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820633
hg1920633
hg1820633
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514002
Supporting Variants
SamplesNA18908
Known GenesGSTM1, GSTM2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2846209
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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