A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126226



Internal ID15979412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3368111..3440355hg38UCSC Ensembl
Innerchr9:3368111..3440355hg19UCSC Ensembl
Innerchr9:3358111..3430355hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3872245
hg1972245
hg1872245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613147
Supporting Variants
Samples
Known GenesRFX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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