A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891928



Internal ID18839638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8959990..9069697hg38UCSC Ensembl
Outerchr11:8959990..9069697hg38UCSC Ensembl
Innerchr11:8981537..9091244hg19UCSC Ensembl
Outerchr11:8981537..9091244hg19UCSC Ensembl
Innerchr11:8938113..9047820hg18UCSC Ensembl
Outerchr11:8938113..9047820hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38109708
hg19109708
hg18109708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790415
Samples
Known GenesNRIP3, SCUBE2, TMEM9B, TMEM9B-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891928
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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