A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891797



Internal ID18839507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45316497..45672399hg38UCSC Ensembl
Outerchr10:45008026..45674466hg38UCSC Ensembl
Innerchr10:45811945..46167847hg19UCSC Ensembl
Outerchr10:45503474..46169914hg19UCSC Ensembl
Innerchr10:45131951..45487853hg18UCSC Ensembl
Outerchr10:44823480..45489920hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38666441
hg19666441
hg18666441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792745, essv25788329
Samples
Known GenesALOX5, ANKRD30BP3, MARCH8, MIR3156-1, OR13A1, RSU1P2, ZFAND4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891797
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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