A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559744



Internal ID16347153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90508106..90731139hg38UCSC Ensembl
Innerchr12:90901883..91124916hg19UCSC Ensembl
Innerchr12:89426014..89649047hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38223034
hg19223034
hg18223034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2782n54
Supporting Variantsnssv800470
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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