A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559225



Internal ID15999948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:69468445..69474630hg38UCSC Ensembl
Innerchr12:69862225..69868410hg19UCSC Ensembl
Innerchr12:68148492..68154677hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg386186
hg196186
hg186186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv797684
Samples
Known GenesFRS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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