A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890979



Internal ID19185375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162038539..162099101hg38UCSC Ensembl
Outerchr6:162038539..162099101hg38UCSC Ensembl
Innerchr6:162459571..162520133hg19UCSC Ensembl
Outerchr6:162459571..162520133hg19UCSC Ensembl
Innerchr6:162379561..162440123hg18UCSC Ensembl
Outerchr6:162379561..162440123hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3860563
hg1960563
hg1860563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786599, essv25787395
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890979
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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