A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562163



Internal ID16349572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68666813..68728486hg38UCSC Ensembl
Innerchr13:69240945..69302618hg19UCSC Ensembl
Innerchr13:68138946..68200619hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3861674
hg1961674
hg1861674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813454
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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