A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561620



Internal ID16349029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49939012..49939828hg38UCSC Ensembl
Innerchr13:50513148..50513964hg19UCSC Ensembl
Innerchr13:49411149..49411965hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38817
hg19817
hg18817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3141n54
Supporting Variantsnssv810371, nssv810370, nssv810369
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561620
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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