A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891756



Internal ID19186152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12265895..12276285hg38UCSC Ensembl
Outerchr10:12260358..12276285hg38UCSC Ensembl
Innerchr10:12307894..12318284hg19UCSC Ensembl
Outerchr10:12302357..12318284hg19UCSC Ensembl
Innerchr10:12347900..12358290hg18UCSC Ensembl
Outerchr10:12342363..12358290hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3815928
hg1915928
hg1815928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801371, essv25794760, essv25800365, essv25801526
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891756
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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