A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561629



Internal ID16349038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49939116..49940570hg38UCSC Ensembl
Innerchr13:50513252..50514706hg19UCSC Ensembl
Innerchr13:49411253..49412707hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381455
hg191455
hg181455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n54
Supporting Variantsnssv810403
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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