A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562554



Internal ID16349963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83973149..84088233hg38UCSC Ensembl
Innerchr13:84547284..84662368hg19UCSC Ensembl
Innerchr13:83445285..83560369hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38115085
hg19115085
hg18115085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816605
Samples
Known GenesMIR548F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562554
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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