A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892113



Internal ID18839823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134302137..134339014hg38UCSC Ensembl
Outerchr11:134299300..134340635hg38UCSC Ensembl
Innerchr11:134172031..134208908hg19UCSC Ensembl
Outerchr11:134169194..134210529hg19UCSC Ensembl
Innerchr11:133677241..133714118hg18UCSC Ensembl
Outerchr11:133674404..133715739hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3841336
hg1941336
hg1841336
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784655, essv25790311
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892113
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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