A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560222



Internal ID16347631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112562881..112574869hg38UCSC Ensembl
Innerchr12:113000685..113012673hg19UCSC Ensembl
Innerchr12:111485068..111497056hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3811989
hg1911989
hg1811989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2875n54
Supporting Variantsnssv802340
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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