A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562798



Internal ID16003521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97433146..97434216hg38UCSC Ensembl
Innerchr13:98085400..98086470hg19UCSC Ensembl
Innerchr13:96883401..96884471hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381071
hg191071
hg181071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3331n54
Supporting Variantsnssv817581
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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