A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890990



Internal ID18838700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162514399..162551207hg38UCSC Ensembl
Outerchr6:162514399..162551207hg38UCSC Ensembl
Innerchr6:162935431..162972239hg19UCSC Ensembl
Outerchr6:162935431..162972239hg19UCSC Ensembl
Innerchr6:162855421..162892229hg18UCSC Ensembl
Outerchr6:162855421..162892229hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3836809
hg1936809
hg1836809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797884
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890990
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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