A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893654



Internal ID18837788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6811906..7026460hg38UCSC Ensembl
Outerchr3:6811906..7026460hg38UCSC Ensembl
Innerchr3:6853593..7068147hg19UCSC Ensembl
Outerchr3:6853593..7068147hg19UCSC Ensembl
Innerchr3:6828593..7043147hg18UCSC Ensembl
Outerchr3:6828593..7043147hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38214555
hg19214555
hg18214555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799514
Samples
Known GenesGRM7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893654
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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