A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560539



Internal ID16001262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124250181..124314841hg38UCSC Ensembl
Innerchr12:124734727..124799387hg19UCSC Ensembl
Innerchr12:123300680..123365340hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3864661
hg1964661
hg1864661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803895
Samples
Known GenesFAM101A, ZNF664-FAM101A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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