A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789872



Internal ID19160296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50366570..50771311hg38UCSC Ensembl
Innerchr11:50325741..50730482hg19UCSC Ensembl
Innerchr11:50282317..50687058hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38404742
hg19404742
hg18404742
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892001
Supporting Variants
Samples
Known GenesLOC646813
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789872
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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