A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891911



Internal ID19186307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3930107..3949182hg38UCSC Ensembl
Outerchr11:3927664..3949182hg38UCSC Ensembl
Innerchr11:3951337..3970412hg19UCSC Ensembl
Outerchr11:3948894..3970412hg19UCSC Ensembl
Innerchr11:3907913..3926988hg18UCSC Ensembl
Outerchr11:3905470..3926988hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3821519
hg1921519
hg1821519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780877, essv25780293, essv25784240, essv25799374
Samples
Known GenesSTIM1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891911
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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