A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553554



Internal ID15994277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13277469..13278110hg38UCSC Ensembl
Innerchr11:13299016..13299657hg19UCSC Ensembl
Innerchr11:13255592..13256233hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38642
hg19642
hg18642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768262
Samples
Known GenesARNTL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553554
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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