A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893597



Internal ID18837731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1004354..1308774hg38UCSC Ensembl
Outerchr3:1004354..1308774hg38UCSC Ensembl
Innerchr3:1046038..1350458hg19UCSC Ensembl
Outerchr3:1046038..1350458hg19UCSC Ensembl
Innerchr3:1021038..1325458hg18UCSC Ensembl
Outerchr3:1021038..1325458hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38304421
hg19304421
hg18304421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790774
Samples
Known GenesCNTN6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893597
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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