A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560105



Internal ID16347514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:108467757..108469087hg38UCSC Ensembl
Innerchr12:108861534..108862864hg19UCSC Ensembl
Innerchr12:107385664..107386994hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381331
hg191331
hg181331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2853n54
Supporting Variantsnssv801912
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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