A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559223



Internal ID16346632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:69466916..69468877hg38UCSC Ensembl
Innerchr12:69860696..69862657hg19UCSC Ensembl
Innerchr12:68146963..68148924hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381962
hg191962
hg181962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv797681
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559223
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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