A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891619



Internal ID19186015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14850258..14996245hg38UCSC Ensembl
Outerchr9:14850258..14996245hg38UCSC Ensembl
Innerchr9:14850256..14996243hg19UCSC Ensembl
Outerchr9:14850256..14996243hg19UCSC Ensembl
Innerchr9:14840256..14986243hg18UCSC Ensembl
Outerchr9:14840256..14986243hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38145988
hg19145988
hg18145988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797251
Samples
Known GenesFREM1, LOC389705
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891619
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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