A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801804



Internal ID15749074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:104135571..104137927hg38UCSC Ensembl
Innerchr12:104529349..104531705hg19UCSC Ensembl
Innerchr12:103053479..103055835hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382357
hg192357
hg182357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560047
Supporting Variants
Samples
Known GenesNFYB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801804
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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