A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892111



Internal ID18839821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132278058..132297744hg38UCSC Ensembl
Outerchr11:132278058..132297744hg38UCSC Ensembl
Innerchr11:132147952..132167638hg19UCSC Ensembl
Outerchr11:132147952..132167638hg19UCSC Ensembl
Innerchr11:131653162..131672848hg18UCSC Ensembl
Outerchr11:131653162..131672848hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3819687
hg1919687
hg1819687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780124
Samples
Known GenesNTM, NTM-IT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892111
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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