A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892109



Internal ID18839819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131358314..131494601hg38UCSC Ensembl
Outerchr11:131358314..131494601hg38UCSC Ensembl
Innerchr11:131228209..131364495hg19UCSC Ensembl
Outerchr11:131228209..131364495hg19UCSC Ensembl
Innerchr11:130733419..130869705hg18UCSC Ensembl
Outerchr11:130733419..130869705hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38136288
hg19136287
hg18136287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780639
Samples
Known GenesNTM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892109
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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