A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615067



Internal ID16402476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104504563..104530716hg38UCSC Ensembl
Innerchr9:107266844..107292997hg19UCSC Ensembl
Innerchr9:106306665..106332818hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3826154
hg1926154
hg1826154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140805
Samples
Known GenesOR13C4, OR13F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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