A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784655



Internal ID18828990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134302137..134340635hg38UCSC Ensembl
Innerchr11:134172031..134210529hg19UCSC Ensembl
Innerchr11:133677241..133715739hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3838499
hg1938499
hg1838499
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892113
Supporting Variants
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784655
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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