A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892025



Internal ID18839735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71675753..71814755hg38UCSC Ensembl
Outerchr11:71570814..71849534hg38UCSC Ensembl
Innerchr11:71386799..71525801hg19UCSC Ensembl
Outerchr11:71281860..71560580hg19UCSC Ensembl
Innerchr11:71064447..71203449hg18UCSC Ensembl
Outerchr11:70959508..71238228hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38278721
hg19278721
hg18278721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791859, essv25791993, essv25792156, essv25790929, essv25791351, essv25792433
Samples
Known GenesALG1L9P, DEFB108B, FAM86C1, KRTAP5-11, ZNF705E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892025
Frequency
Sample Size3017
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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