A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560220



Internal ID16347629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112557960..112574711hg38UCSC Ensembl
Innerchr12:112995764..113012515hg19UCSC Ensembl
Innerchr12:111480147..111496898hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3816752
hg1916752
hg1816752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2875n54
Supporting Variantsnssv802337
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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