A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2829228



Internal ID15417279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36175569..36196796hg38UCSC Ensembl
Innerchr17:34502929..34524195hg19UCSC Ensembl
Innerchr17:31527042..31548308hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3821228
hg1921267
hg1821267
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514837
Supporting Variants
SamplesNA19208
Known GenesCCL3L1, CCL3L3, TBC1D3B
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2829228
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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