A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791613



Internal ID18824156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133432340..133524462hg38UCSC Ensembl
Innerchr10:135245844..135337966hg19UCSC Ensembl
Innerchr10:135095834..135187956hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3892123
hg1992123
hg1892123
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891902
Supporting Variants
Samples
Known GenesSCART1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791613
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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