A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893789



Internal ID19184609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153892457..153902233hg38UCSC Ensembl
Outerchr3:153892457..153902233hg38UCSC Ensembl
Innerchr3:153610246..153620022hg19UCSC Ensembl
Outerchr3:153610246..153620022hg19UCSC Ensembl
Innerchr3:155092936..155102712hg18UCSC Ensembl
Outerchr3:155092936..155102712hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg389777
hg199777
hg189777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785908
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893789
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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