A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560170



Internal ID16000893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111380897..111444681hg38UCSC Ensembl
Innerchr12:111818701..111882485hg19UCSC Ensembl
Innerchr12:110303084..110366868hg18UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3863785
hg1963785
hg1863785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv802025
Samples
Known GenesSH2B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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