A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768248



Internal ID15715518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12244951..12261361hg38UCSC Ensembl
Innerchr11:12266498..12282908hg19UCSC Ensembl
Innerchr11:12223074..12239484hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3816411
hg1916411
hg1816411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553546
Supporting Variants
Samples
Known GenesMICAL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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