A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560453



Internal ID16001176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:120904383..120926521hg38UCSC Ensembl
Innerchr12:121342186..121364324hg19UCSC Ensembl
Innerchr12:119826569..119848707hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3822139
hg1922139
hg1822139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2918n54
Supporting Variantsnssv803426
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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