A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560389



Internal ID16001112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:118064662..118126282hg38UCSC Ensembl
Innerchr12:118502467..118564087hg19UCSC Ensembl
Innerchr12:116986850..117048470hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3861621
hg1961621
hg1861621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803308
Samples
Known GenesVSIG10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560389
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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