A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559220



Internal ID16346629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:68858935..68862663hg38UCSC Ensembl
Innerchr12:69252715..69256443hg19UCSC Ensembl
Innerchr12:67538982..67542710hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383729
hg193729
hg183729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv797588
Samples
Known GenesCPM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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