A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656866



Internal ID15046832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162120674..162828613hg38UCSC Ensembl
Innerchr6:162541706..163249645hg19UCSC Ensembl
Innerchr6:162461696..163169635hg18UCSC Ensembl
Innerchr6:162512117..163220056hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38707940
hg19707940
hg18707940
hg17707940
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)nssv656866
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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