A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891715



Internal ID18839425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113098921..113122780hg38UCSC Ensembl
Outerchr9:113098921..113122780hg38UCSC Ensembl
Innerchr9:115861201..115885060hg19UCSC Ensembl
Outerchr9:115861201..115885060hg19UCSC Ensembl
Innerchr9:114901022..114924881hg18UCSC Ensembl
Outerchr9:114901022..114924881hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3823860
hg1923860
hg1823860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788048
Samples
Known GenesFAM225A, FAM225B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891715
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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