A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890978



Internal ID18838688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161452979..161535643hg38UCSC Ensembl
Outerchr6:161452979..161535643hg38UCSC Ensembl
Innerchr6:161874011..161956675hg19UCSC Ensembl
Outerchr6:161874011..161956675hg19UCSC Ensembl
Innerchr6:161794001..161876665hg18UCSC Ensembl
Outerchr6:161794001..161876665hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3882665
hg1982665
hg1882665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782960
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890978
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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