A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891708



Internal ID19186104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107855817..107895834hg38UCSC Ensembl
Outerchr9:107855817..107895834hg38UCSC Ensembl
Innerchr9:110618098..110658115hg19UCSC Ensembl
Outerchr9:110618098..110658115hg19UCSC Ensembl
Innerchr9:109657919..109697936hg18UCSC Ensembl
Outerchr9:109657919..109697936hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3840018
hg1940018
hg1840018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789866
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891708
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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