A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562198



Internal ID16349607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68850619..68882822hg38UCSC Ensembl
Innerchr13:69424751..69456954hg19UCSC Ensembl
Innerchr13:68322752..68354955hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3832204
hg1932204
hg1832204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813686
Samples
Known GenesLINC00550, MIR548H4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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