A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561110



Internal ID16001833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132630826..132677497hg38UCSC Ensembl
Innerchr12:133207412..133254083hg19UCSC Ensembl
Innerchr12:131717485..131764156hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3846672
hg1946672
hg1846672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv805916
Samples
Known GenesPOLE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561110
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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