A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891661



Internal ID19186057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38673915..38997694hg38UCSC Ensembl
Outerchr9:38673915..39038231hg38UCSC Ensembl
Innerchr9:38673912..38997691hg19UCSC Ensembl
Outerchr9:38673912..39038228hg19UCSC Ensembl
Innerchr9:38663912..38987691hg18UCSC Ensembl
Outerchr9:38663912..39028228hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38364317
hg19364317
hg18364317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790896, essv25791466
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891661
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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