A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891723



Internal ID19186119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118732620..118784110hg38UCSC Ensembl
Outerchr9:118732620..118784110hg38UCSC Ensembl
Innerchr9:121494898..121546388hg19UCSC Ensembl
Outerchr9:121494898..121546388hg19UCSC Ensembl
Innerchr9:120534719..120586209hg18UCSC Ensembl
Outerchr9:120534719..120586209hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3851491
hg1951491
hg1851491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779631
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891723
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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