A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890987



Internal ID18838697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162085536..162250307hg38UCSC Ensembl
Outerchr6:162085536..162250307hg38UCSC Ensembl
Innerchr6:162506568..162671339hg19UCSC Ensembl
Outerchr6:162506568..162671339hg19UCSC Ensembl
Innerchr6:162426558..162591329hg18UCSC Ensembl
Outerchr6:162426558..162591329hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38164772
hg19164772
hg18164772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785962
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890987
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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