A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615226



Internal ID16055949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114139646..114162501hg38UCSC Ensembl
Innerchr9:116901926..116924781hg19UCSC Ensembl
Innerchr9:115941747..115964602hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3822856
hg1922856
hg1822856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12856n54
Supporting Variantsnssv1141261
Samples
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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