A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563088



Internal ID16350497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109781963..109787931hg38UCSC Ensembl
Innerchr13:110434310..110440278hg19UCSC Ensembl
Innerchr13:109232311..109238279hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385969
hg195969
hg185969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819715
Samples
Known GenesIRS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563088
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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