A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075576



Internal ID15582076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162673891..162791267hg38UCSC Ensembl
Innerchr6:163094923..163212299hg19UCSC Ensembl
Innerchr6:163014913..163132289hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38117377
hg19117377
hg18117377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605180
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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