A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890984



Internal ID18838694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162239956..162485562hg38UCSC Ensembl
Outerchr6:162203614..162629816hg38UCSC Ensembl
Innerchr6:162660988..162906594hg19UCSC Ensembl
Outerchr6:162624646..163050848hg19UCSC Ensembl
Innerchr6:162580978..162826584hg18UCSC Ensembl
Outerchr6:162544636..162970838hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38426203
hg19426203
hg18426203
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788036, essv25798045
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890984
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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