A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891964



Internal ID19186360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36166245..36205009hg38UCSC Ensembl
Outerchr11:36134028..36212201hg38UCSC Ensembl
Innerchr11:36187795..36226559hg19UCSC Ensembl
Outerchr11:36155578..36233751hg19UCSC Ensembl
Innerchr11:36144371..36183135hg18UCSC Ensembl
Outerchr11:36112154..36190327hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3878174
hg1978174
hg1878174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781972, essv25782312
Samples
Known GenesLDLRAD3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891964
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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