A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779934



Internal ID19182520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103591783..103755481hg38UCSC Ensembl
Innerchr11:103462511..103626209hg19UCSC Ensembl
Innerchr11:102967721..103131419hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38163699
hg19163699
hg18163699
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892095
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779934
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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