A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779631



Internal ID19169923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118732620..118784110hg38UCSC Ensembl
Innerchr9:121494898..121546388hg19UCSC Ensembl
Innerchr9:120534719..120586209hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3851491
hg1951491
hg1851491
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891723
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779631
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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