A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560093



Internal ID16347502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:107986225..108082360hg38UCSC Ensembl
Innerchr12:108380002..108476137hg19UCSC Ensembl
Innerchr12:106904132..107000267hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3896136
hg1996136
hg1896136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2851n54
Supporting Variantsnssv801898
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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