A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562202



Internal ID16349611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68965050..69016545hg38UCSC Ensembl
Innerchr13:69539182..69590677hg19UCSC Ensembl
Innerchr13:68437183..68488678hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3851496
hg1951496
hg1851496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175984
Samples1780862380_A
Known GenesMIR548H4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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