A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792745



Internal ID18815186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45008026..45674466hg38UCSC Ensembl
Innerchr10:45503474..46169914hg19UCSC Ensembl
Innerchr10:44823480..45489920hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38666441
hg19666441
hg18666441
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891797
Supporting Variants
Samples
Known GenesALOX5, ANKRD30BP3, MARCH8, MIR3156-1, OR13A1, RSU1P2, ZFAND4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=121
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792745
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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