A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778391



Internal ID18813786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89730855..90041084hg38UCSC Ensembl
Innerchr11:89464023..89774252hg19UCSC Ensembl
Innerchr11:89103671..89413900hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38310230
hg19310230
hg18310230
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892056
Supporting Variants
Samples
Known GenesMIR5692A1, TRIM49, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=61
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778391
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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