A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2829778



Internal ID15359315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36089065..36168713hg38UCSC Ensembl
Innerchr17:34416411..34496071hg19UCSC Ensembl
Innerchr17:31440524..31520184hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3879649
hg1979661
hg1879661
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514836
Supporting Variants
SamplesNA18934
Known GenesCCL3, CCL4, TBC1D3B
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2829778
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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