A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563321



Internal ID16004044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113369086..113452383hg38UCSC Ensembl
Innerchr13:114023401..114106698hg19UCSC Ensembl
Innerchr13:113071402..113154699hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3883298
hg1983298
hg1883298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820524
Samples
Known GenesADPRHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563321
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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