A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563301



Internal ID16350710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113167116..113168636hg38UCSC Ensembl
Innerchr13:113821430..113822950hg19UCSC Ensembl
Innerchr13:112869431..112870951hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381521
hg191521
hg181521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820487
Samples
Known GenesPROZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563301
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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