A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892383



Internal ID19183203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68814644..68875299hg38UCSC Ensembl
Outerchr13:68814644..68875299hg38UCSC Ensembl
Innerchr13:69388776..69449431hg19UCSC Ensembl
Outerchr13:69388776..69449431hg19UCSC Ensembl
Innerchr13:68286777..68347432hg18UCSC Ensembl
Outerchr13:68286777..68347432hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3860656
hg1960656
hg1860656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788520
Samples
Known GenesLINC00550, MIR548H4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892383
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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