A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613145



Internal ID16053868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3237378..3349487hg38UCSC Ensembl
Innerchr9:3237378..3349487hg19UCSC Ensembl
Innerchr9:3227378..3339487hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38112110
hg19112110
hg18112110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126225
Samples
Known GenesRFX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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