A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562980



Internal ID16003703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102582273..102619667hg38UCSC Ensembl
Innerchr13:103234623..103272017hg19UCSC Ensembl
Innerchr13:102032624..102070018hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3837395
hg1937395
hg1837395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818820
Samples
Known GenesTPP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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