A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797251



Internal ID19162668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14850258..14996245hg38UCSC Ensembl
Innerchr9:14850256..14996243hg19UCSC Ensembl
Innerchr9:14840256..14986243hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38145988
hg19145988
hg18145988
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891619
Supporting Variants
Samples
Known GenesFREM1, LOC389705
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797251
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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