A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560263



Internal ID16347672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112926577..112929077hg38UCSC Ensembl
Innerchr12:113364382..113366882hg19UCSC Ensembl
Innerchr12:111848765..111851265hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg382501
hg192501
hg182501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv802724
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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