A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891631



Internal ID19186027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19840699..19882456hg38UCSC Ensembl
Outerchr9:19827261..19882456hg38UCSC Ensembl
Innerchr9:19840697..19882454hg19UCSC Ensembl
Outerchr9:19827259..19882454hg19UCSC Ensembl
Innerchr9:19830697..19872454hg18UCSC Ensembl
Outerchr9:19817259..19872454hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3855196
hg1955196
hg1855196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784675, essv25800703
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891631
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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