A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893855



Internal ID18837989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197959451..198097000hg38UCSC Ensembl
Outerchr3:197912510..198111391hg38UCSC Ensembl
Innerchr3:197686322..197823871hg19UCSC Ensembl
Outerchr3:197639381..197838262hg19UCSC Ensembl
Innerchr3:199170719..199308268hg18UCSC Ensembl
Outerchr3:199123778..199322659hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38198882
hg19198882
hg18198882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788235, essv25792900, essv25791226, essv25790723, essv25791617
Samples
Known GenesANKRD18DP, IQCG, LMLN, RPL35A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893855
Frequency
Sample Size3017
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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