A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891618



Internal ID19186014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13812038..13865260hg38UCSC Ensembl
Outerchr9:13812038..13865260hg38UCSC Ensembl
Innerchr9:13812037..13865259hg19UCSC Ensembl
Outerchr9:13812037..13865259hg19UCSC Ensembl
Innerchr9:13802037..13855259hg18UCSC Ensembl
Outerchr9:13802037..13855259hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3853223
hg1953223
hg1853223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796898
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891618
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer