A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559426



Internal ID16346835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:77137870..77197636hg38UCSC Ensembl
Innerchr12:77531650..77591416hg19UCSC Ensembl
Innerchr12:76055781..76115547hg18UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3859767
hg1959767
hg1859767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv798868
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559426
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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