A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013114



Internal ID19102332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177703667..177726180hg38UCSC Ensembl
Innerchr3:177421455..177443968hg19UCSC Ensembl
Innerchr3:178904149..178926662hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3822514
hg1922514
hg1822514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614981
Samples
Known GenesLINC00578
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013114
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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