A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789975



Internal ID19160422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24457293..24491589hg38UCSC Ensembl
Innerchr9:24457291..24491587hg19UCSC Ensembl
Innerchr9:24447291..24481587hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3834297
hg1934297
hg1834297
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891641
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789975
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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