A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768263



Internal ID15715533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13277572..13278110hg38UCSC Ensembl
Innerchr11:13299119..13299657hg19UCSC Ensembl
Innerchr11:13255695..13256233hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38539
hg19539
hg18539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553555
Supporting Variants
Samples
Known GenesARNTL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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