A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891916



Internal ID19186312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5169244..5227774hg38UCSC Ensembl
Outerchr11:5169244..5227774hg38UCSC Ensembl
Innerchr11:5190474..5249004hg19UCSC Ensembl
Outerchr11:5190474..5249004hg19UCSC Ensembl
Innerchr11:5147050..5205580hg18UCSC Ensembl
Outerchr11:5147050..5205580hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3858531
hg1958531
hg1858531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780724, essv25780582
Samples
Known GenesHBB, OR51V1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891916
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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