A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789347



Internal ID19166556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6027173..6094747hg38UCSC Ensembl
Innerchr3:6068860..6136434hg19UCSC Ensembl
Innerchr3:6043860..6111434hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3867575
hg1967575
hg1867575
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893650
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789347
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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