A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891709



Internal ID19186105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110400024..110415044hg38UCSC Ensembl
Outerchr9:110400024..110415044hg38UCSC Ensembl
Innerchr9:113162304..113177324hg19UCSC Ensembl
Outerchr9:113162304..113177324hg19UCSC Ensembl
Innerchr9:112202125..112217145hg18UCSC Ensembl
Outerchr9:112202125..112217145hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3815021
hg1915021
hg1815021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800220
Samples
Known GenesSVEP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891709
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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