A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891731



Internal ID19186127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133071778..133080285hg38UCSC Ensembl
Outerchr9:133066817..133082065hg38UCSC Ensembl
Innerchr9:135947165..135955672hg19UCSC Ensembl
Outerchr9:135942204..135957452hg19UCSC Ensembl
Innerchr9:134936986..134945493hg18UCSC Ensembl
Outerchr9:134932025..134947273hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3815249
hg1915249
hg1815249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787163, essv25780523, essv25779266, essv25796335
Samples
Known GenesCEL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891731
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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