A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563380



Internal ID16004103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113540846..113610202hg38UCSC Ensembl
Innerchr13:114195161..114264517hg19UCSC Ensembl
Innerchr13:113243162..113312518hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3869357
hg1969357
hg1869357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149463
Samples1780862275_A
Known GenesTFDP1, TMCO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563380
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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