A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790774



Internal ID18826911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1004354..1308774hg38UCSC Ensembl
Innerchr3:1046038..1350458hg19UCSC Ensembl
Innerchr3:1021038..1325458hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38304421
hg19304421
hg18304421
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893597
Supporting Variants
Samples
Known GenesCNTN6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=154
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790774
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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