A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891753



Internal ID19186149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9101548..9150641hg38UCSC Ensembl
Outerchr10:9097436..9158139hg38UCSC Ensembl
Innerchr10:9143511..9192604hg19UCSC Ensembl
Outerchr10:9139399..9200102hg19UCSC Ensembl
Innerchr10:9183517..9232610hg18UCSC Ensembl
Outerchr10:9179405..9240108hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3860704
hg1960704
hg1860704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796764, essv25796973, essv25781382
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891753
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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