A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075564



Internal ID15582064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162452461..162619450hg38UCSC Ensembl
Innerchr6:162873493..163040482hg19UCSC Ensembl
Innerchr6:162793483..162960472hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38166990
hg19166990
hg18166990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605167
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075564
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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