A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020298



Internal ID19109517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14277254..14294981hg38UCSC Ensembl
Innerchr9:14277253..14294980hg19UCSC Ensembl
Innerchr9:14267253..14284980hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3817728
hg1917728
hg1817728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690618
Samples
Known GenesNFIB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020298
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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