A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560467



Internal ID16001190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:121747352..121748051hg38UCSC Ensembl
Innerchr12:122185258..122185957hg19UCSC Ensembl
Innerchr12:120669641..120670340hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2920n54
Supporting Variantsnssv803475, nssv803480, nssv803479, nssv803482, nssv803481, nssv803474, nssv803477, nssv803478, nssv803476
Samples
Known GenesTMEM120B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560467
Frequency
Sample Size17421
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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