A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892001



Internal ID19186397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50366570..50683379hg38UCSC Ensembl
Outerchr11:50360886..50771311hg38UCSC Ensembl
Innerchr11:50325741..50642550hg19UCSC Ensembl
Outerchr11:50320057..50730482hg19UCSC Ensembl
Innerchr11:50282317..50599126hg18UCSC Ensembl
Outerchr11:50276633..50687058hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38410426
hg19410426
hg18410426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789872, essv25792860
Samples
Known GenesLOC646813
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892001
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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