A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561570



Internal ID16348979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43167710..43213511hg38UCSC Ensembl
Innerchr13:43741846..43787647hg19UCSC Ensembl
Innerchr13:42639846..42685647hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3845802
hg1945802
hg1845802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3133n54
Supporting Variantsnssv809971, nssv809972
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561570
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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