A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686795



Internal ID15076761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162354823..162741318hg38UCSC Ensembl
Innerchr6:162775855..163162350hg19UCSC Ensembl
Innerchr6:162695845..163082340hg18UCSC Ensembl
Innerchr6:162746266..163132761hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38386496
hg19386496
hg18386496
hg17386496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686795
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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