A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791466



Internal ID19160464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38673915..38997694hg38UCSC Ensembl
Innerchr9:38673912..38997691hg19UCSC Ensembl
Innerchr9:38663912..38987691hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38323780
hg19323780
hg18323780
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891661
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=53
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791466
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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