A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605119



Internal ID16045842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162214013..162315444hg38UCSC Ensembl
Innerchr6:162635045..162736476hg19UCSC Ensembl
Innerchr6:162555035..162656466hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38101432
hg19101432
hg18101432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075522
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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