A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553988



Internal ID15994711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31513808..31629642hg38UCSC Ensembl
Innerchr11:31535355..31651189hg19UCSC Ensembl
Innerchr11:31491931..31607765hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38115835
hg19115835
hg18115835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771046
Samples
Known GenesELP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553988
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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