A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891718



Internal ID19186114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115855252..115903186hg38UCSC Ensembl
Outerchr9:115855252..115903186hg38UCSC Ensembl
Innerchr9:118617531..118665465hg19UCSC Ensembl
Outerchr9:118617531..118665465hg19UCSC Ensembl
Innerchr9:117657352..117705286hg18UCSC Ensembl
Outerchr9:117657352..117705286hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3847935
hg1947935
hg1847935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799669
Samples
Known GenesLINC00474
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891718
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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