A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29980



Internal ID5921842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1820597..2097889hg38UCSC Ensembl
Innerchr11:1841827..2119119hg19UCSC Ensembl
Innerchr11:1798403..2075695hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38277293
hg19277293
hg18277293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84219
SamplesHuRef
Known GenesH19, LSP1, MIR4298, MIR675, MRPL23, MRPL23-AS1, SYT8, TNNI2, TNNT3
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29980
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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