A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786362



Internal ID15733632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:1593541..1594567hg38UCSC Ensembl
Innerchr12:1702707..1703733hg19UCSC Ensembl
Innerchr12:1572968..1573994hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381027
hg191027
hg181027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556987
Supporting Variants
Samples
Known GenesFBXL14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv786362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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