A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560094



Internal ID16347503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:107986225..108095158hg38UCSC Ensembl
Innerchr12:108380002..108488935hg19UCSC Ensembl
Innerchr12:106904132..107013065hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38108934
hg19108934
hg18108934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2851n54
Supporting Variantsnssv1176430
Samples1780862095_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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