A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892604



Internal ID18836738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22846220..22996179hg38UCSC Ensembl
Outerchr15:22721590..23121326hg38UCSC Ensembl
Innerchr15:22876889..23026848hg19UCSC Ensembl
Outerchr15:22751742..23151516hg19UCSC Ensembl
Innerchr15:20428330..20578289hg18UCSC Ensembl
Outerchr15:20303106..20702957hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38399737
hg19399775
hg18399852
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782845, essv25789182, essv25789315, essv25782812, essv25801351, essv25800766, essv25784906, essv25799766, essv25784194, essv25791948, essv25788685, essv25782515, essv25780062, essv25789014, essv25787003, essv25789106
Samples
Known GenesCYFIP1, LOC283683, NIPA1, NIPA2, TUBGCP5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892604
Frequency
Sample Size3017
Observed Gain6
Observed Loss10
Observed Complex0
Frequencyn/a


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