A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893831



Internal ID19184651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181810241..181874886hg38UCSC Ensembl
Outerchr3:181810241..181874886hg38UCSC Ensembl
Innerchr3:181528029..181592674hg19UCSC Ensembl
Outerchr3:181528029..181592674hg19UCSC Ensembl
Innerchr3:183010723..183075368hg18UCSC Ensembl
Outerchr3:183010723..183075368hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3864646
hg1964646
hg1864646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787582
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893831
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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