A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561015



Internal ID16348424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132387668..132430955hg38UCSC Ensembl
Innerchr12:132964254..133007541hg19UCSC Ensembl
Innerchr12:131474327..131517614hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3843288
hg1943288
hg1843288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv805629
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561015
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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