A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560374



Internal ID16001097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:117203981..117213068hg38UCSC Ensembl
Innerchr12:117641786..117650873hg19UCSC Ensembl
Innerchr12:116126169..116135256hg18UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg389088
hg199088
hg189088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2903n54
Supporting Variantsnssv803283, nssv803285, nssv803284, nssv803286
Samples
Known GenesNOS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560374
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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