A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562096



Internal ID16349505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66129578..66224791hg38UCSC Ensembl
Innerchr13:66703710..66798923hg19UCSC Ensembl
Innerchr13:65601711..65696924hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3895214
hg1995214
hg1895214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813155
Samples
Known GenesMIR4704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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