A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801939



Internal ID15749209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109702295..109714679hg38UCSC Ensembl
Innerchr12:110140100..110152484hg19UCSC Ensembl
Innerchr12:108624483..108636867hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3812385
hg1912385
hg1812385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560122
Supporting Variants
Samples
Known GenesFAM222A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801939
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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