A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047866



Internal ID19137085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116760866..116778355hg38UCSC Ensembl
Innerchr9:119523145..119540634hg19UCSC Ensembl
Innerchr9:118562966..118580455hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3817490
hg1917490
hg1817490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695190
Samples
Known GenesASTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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