A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792440



Internal ID19179097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95138313..95359375hg38UCSC Ensembl
Innerchr3:94857157..95078219hg19UCSC Ensembl
Innerchr3:96339847..96560909hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38221063
hg19221063
hg18221063
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893748
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792440
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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