A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893769



Internal ID19184589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114923561..114949049hg38UCSC Ensembl
Outerchr3:114923561..114949049hg38UCSC Ensembl
Innerchr3:114642408..114667896hg19UCSC Ensembl
Outerchr3:114642408..114667896hg19UCSC Ensembl
Innerchr3:116125098..116150586hg18UCSC Ensembl
Outerchr3:116125098..116150586hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3825489
hg1925489
hg1825489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783963, essv25784699
Samples
Known GenesZBTB20
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893769
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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