A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891932



Internal ID18839642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15010551..15174410hg38UCSC Ensembl
Outerchr11:15010551..15174410hg38UCSC Ensembl
Innerchr11:15032097..15195956hg19UCSC Ensembl
Outerchr11:15032097..15195956hg19UCSC Ensembl
Innerchr11:14988673..15152532hg18UCSC Ensembl
Outerchr11:14988673..15152532hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38163860
hg19163860
hg18163860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791272
Samples
Known GenesCALCB, INSC
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891932
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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