A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560385



Internal ID16347794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:117348300..117408001hg38UCSC Ensembl
Innerchr12:117786105..117845806hg19UCSC Ensembl
Innerchr12:116270488..116330189hg18UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg3859702
hg1959702
hg1859702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803304
Samples
Known GenesNOS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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