A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891967



Internal ID19186363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38145652..38202551hg38UCSC Ensembl
Outerchr11:38145652..38202551hg38UCSC Ensembl
Innerchr11:38167202..38224101hg19UCSC Ensembl
Outerchr11:38167202..38224101hg19UCSC Ensembl
Innerchr11:38123778..38180677hg18UCSC Ensembl
Outerchr11:38123778..38180677hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3856900
hg1956900
hg1856900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790048
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891967
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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