A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790410



Internal ID19172661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21378570..21428963hg38UCSC Ensembl
Innerchr11:21400116..21450509hg19UCSC Ensembl
Innerchr11:21356692..21407085hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3850394
hg1950394
hg1850394
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891944
Supporting Variants
Samples
Known GenesNELL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790410
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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