A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891789



Internal ID18839499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42298677..42443698hg38UCSC Ensembl
Outerchr10:42288033..42543739hg38UCSC Ensembl
Innerchr10:42794125..42939146hg19UCSC Ensembl
Outerchr10:42783481..43039187hg19UCSC Ensembl
Innerchr10:42114131..42259152hg18UCSC Ensembl
Outerchr10:42103487..42359193hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38255707
hg19255707
hg18255707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789250, essv25788754, essv25789330, essv25790794, essv25788781, essv25789855
Samples
Known GenesCCNYL2, LINC00839, LOC441666, ZNF37BP
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891789
Frequency
Sample Size3017
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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