A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563000



Internal ID16350409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105547959..105664629hg38UCSC Ensembl
Innerchr13:106200308..106316978hg19UCSC Ensembl
Innerchr13:104998309..105114979hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38116671
hg19116671
hg18116671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818849
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563000
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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