A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791921



Internal ID18831578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29906486..31116345hg38UCSC Ensembl
Innerchr9:29906484..31116343hg19UCSC Ensembl
Innerchr9:29896484..31106343hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381209860
hg191209860
hg181209860
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891652
Supporting Variants
Samples
Known GenesLOC401497
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=267
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791921
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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