A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018389



Internal ID18760922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11596157..11633767hg38UCSC Ensembl
Innerchr9:11596157..11633767hg19UCSC Ensembl
Innerchr9:11586157..11623767hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3837611
hg1937611
hg1837611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689240
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018389
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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