A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891972



Internal ID18839682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42842734..43307064hg38UCSC Ensembl
Outerchr11:42842734..43307064hg38UCSC Ensembl
Innerchr11:42864284..43328614hg19UCSC Ensembl
Outerchr11:42864284..43328614hg19UCSC Ensembl
Innerchr11:42820860..43285190hg18UCSC Ensembl
Outerchr11:42820860..43285190hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38464331
hg19464331
hg18464331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791838
Samples
Known GenesHNRNPKP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891972
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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