A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801035



Internal ID18819049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176316166..176329340hg38UCSC Ensembl
Innerchr4:177237317..177250491hg19UCSC Ensembl
Innerchr4:177474311..177487485hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3813175
hg1913175
hg1813175
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894072
Supporting Variants
Samples
Known GenesSPCS3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801035
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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