A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893757



Internal ID19184577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103292443..103461553hg38UCSC Ensembl
Outerchr3:103292443..103461553hg38UCSC Ensembl
Innerchr3:103011287..103180397hg19UCSC Ensembl
Outerchr3:103011287..103180397hg19UCSC Ensembl
Innerchr3:104493977..104663087hg18UCSC Ensembl
Outerchr3:104493977..104663087hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38169111
hg19169111
hg18169111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778233
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893757
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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