A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586004



Internal ID7057386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61647899hg38UCSC Ensembl
Innerchr9:44727847..44855737hg19UCSC Ensembl
Innerchr9:44667843..44795733hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38127891
hg19127891
hg18127891
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994373
Supporting Variants
SamplesHuRef
Known Genes
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586004
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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