A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562796



Internal ID16003519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97433070..97434216hg38UCSC Ensembl
Innerchr13:98085324..98086470hg19UCSC Ensembl
Innerchr13:96883325..96884471hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381147
hg191147
hg181147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3331n54
Supporting Variantsnssv817578, nssv817579
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562796
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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